Bcma binding molecules and methods of use thereof

ABSTRACT

The invention provides antibodies, antigen binding fragments thereof, chimeric antigen receptors (CARs), and engineered T cell receptors, polynucleotides encoding the same, and in vitro cells comprising the same. The polynucleotides, polypeptides, and in vitro cells described herein can be used in an engineered CAR T cell therapy for the treatment of a patient suffering from a cancer. In one embodiment, the polynucleotides, polypeptides, and in vitro cells described herein can be used for the treatment of multiple myeloma.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 16/569,341, filed Sep. 12, 2019, now U.S. Pat. No. 11,505,613, which is a continuation of U.S. application Ser. No. 15/476,309, filed Mar. 31, 2017, now U.S. Pat. No. 10,689,450, and claims the benefit of U.S. Provisional Patent Application No. 62/317,334, filed Apr. 1, 2016, all of which are hereby incorporated by reference in their entireties.

REFERENCE TO AN ELECTRONIC SEQUENCE LISTING

The contents of the electronic sequence listing (76NT-353593-US3.xml; Size: 670,804 bytes; and Date of Creation: Jan. 12, 2023) is herein incorporated by reference in its entirety.

FIELD OF THE INVENTION

This invention relates to chimeric antigen receptors (CARs) and engineered T cell receptors (TCRs) comprising an antigen binding molecule which binds to B-cell maturation antigen (BCMA), polynucleotides encoding the same, and methods of treating a cancer or other disease or disorder in a patient using the same.

BACKGROUND OF THE INVENTION

Human cancers are by their nature comprised of normal cells that have undergone a genetic or epigenetic conversion to become abnormal cancer cells. In doing so, cancer cells begin to express proteins and other antigens that are distinct from those expressed by normal cells. These aberrant tumor antigens can be used by the body's innate immune system to specifically target and kill cancer cells. However, cancer cells employ various mechanisms to prevent immune cells, such as T and B lymphocytes, from successfully targeting cancer cells.

Human T cell therapies rely on enriched or modified human T cells to target and kill cancer cells in a patient. To increase the ability of T cells to target and kill a particular cancer cell, methods have been developed to engineer T cells to express constructs which direct T cells to a particular target cancer cell. Chimeric antigen receptors (CARs) and engineered T cell receptors (TCRs), which comprise binding domains capable of interacting with a particular tumor antigen, allow T cells to target and kill cancer cells that express the particular tumor antigen.

Current therapies for hematologic malignancies have shown varying levels of effectiveness with undesired side effects. Therefore, a need exists to identify novel and improved therapies for treating BCMA related diseases and disorders.

SUMMARY OF THE INVENTION

The present invention is directed to an isolated polynucleotide encoding a chimeric antigen receptor (CAR) or T cell receptor (TCR) comprising a binding molecule that specifically binds to B-cell maturation antigen (BCMA), wherein the binding molecule comprises: (a) a heavy chain variable region (VH) complementarity determining region (CDR) 1 comprising, consisting of, or consisting essentially of the amino acid sequence GX₂X₃X₄X₅X₆X₇SY (SEQ ID NO: 145) wherein: X₂ is not present or G; X₃ is not present or S; X₄ is F, G, I, or Y; X₅ is S or T; X₆ is F or S; and X₇ is S or T; and/or (b) a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁₁X₃X₄X₅X₆X₇X₈X₉X₁₀YX₁₂X₁₃X₁₄X₁₅X₁₆X₁₇ (SEQ ID NO: 146), wherein: X₁ is A, G, I, S, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is not present or G or S; X₈ is N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₂ is A or N; X₁₃ is D, P, or Q; X₁₄ is K or S; X₁₅ is F, L, or V; X₁₆ is K or Q; and X₁₇ is G or S; and/or (c) a VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇DX₁₉ (SEQ ID NO: 147), wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or A, D, G, P, R, or S; X₅ is not present or E, F, G, L, Q, or T; X₆ is not present or E, M, Q, W, or Y; X₇ is not present or A, E, L, or S; X₈ is not present or G, P, S, or T; X₉ is not present or G, P, or S; X₁₀ is not present or I, L, P, or Y; X₁₁ is not present or W; X₁₂ is not present or H; X₁₃ is not present or E or Y; X₁₄ is not present or D, G, H, P, S, W, or Y; X₁₅ is A, G, L, W, or Y; X₁₆ is not present or A, G, I, P, or V; X₁₇ is F, L, or M; and X₁₉ is I, L, V, or Y; and/or (d) a light chain variable region (VL) CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SQX₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅LX₁₇ (SEQ ID NO: 148), wherein X₁ is K or R; X₂ is A or S; X₅ is G or S; X₆ is I, L, or V; X₇ is L or S; X₈ is not present or H or Y; X₉ is not present or S; X₁₀ is not present or N or S; X₁₁ is not present or G or N; X₁₂ is not present or N; X₁₃ is not present or K or Y; X₁₄ is N, R, or S; X₁₅ is N, W, or Y; and X₁₇ is A or D; (e) a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SX₄X₅X₆X₇(SEQ ID NO: 149), wherein X₁ is D, G, L, S, or W; X₂ is A or G; X₄ is N, S, or T; X₅ is L or R; X₆ is A, E, or Q; and X₇ is S or T; and/or (f) a VL CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁QX₃X₄X₅X₆PX₈T (SEQ ID NO: 150), wherein X₁ is M or Q; X₃ is F, G, H, I, R, or Y; X₄ is A, F, H, I, L, or Y; X₅ is A, G, H, S, T, V, or Y; X₆ is F, L, T, W, or Y; and X₈ is not present or F, L, P, or W.

In another embodiment, the invention is directed to an isolated polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, wherein the antibody or the antigen binding molecule thereof comprises: (a) a heavy chain variable region (VH) complementarity determining region (CDR) 1 comprising, consisting of, or consisting essentially of the amino acid sequence GX₂X₃X₄X₅X₆X₇SY (SEQ ID NO: 145), wherein: X₂ is not present or G; X₃ is not present or S; X₄ is F, G, I, or Y; X₅ is S or T; X₆ is F or S; and X₇ is S or T; and/or (b) a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃X₄X₅X₆X₇X₈X₉X₁₀YX₁₂X₁₃X₁₄X₁₅X₁₆X₁₇ (SEQ ID NO: 146), wherein: X₁ is A, G, I, S, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is not present or G or S; X₈ is N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₂ is A or N; X₁₃ is D, P, or Q; X₁₄ is K or S; X₁₅ is F, L, or V; X₁₆ is K or Q; and X₁₇ is G or S; and/or (c) a VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇DX₁₉ (SEQ ID NO: 147), wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or A, D, G, P, R, or S; X₅ is not present or E, F, G, L, Q, or T; X₆ is not present or E, M, Q, W, or Y; X₇ is not present or A, E, L, or S; X₈ is not present or G, P, S, or T; X₉ is not present or G, P, or S; X₁₀ is not present or I, L, P, or Y; X₁₁ is not present or W; X₁₂ is not present or H; X₁₃ is not present or E or Y; X₁₄ is not present or D, G, H, P, S, W, or Y; X₁₅ is A, G, L, W, or Y; X₁₆ is not present or A, G, I, P, or V; X₁₇ is F, L, or M; and X₁₉ is I, L, V, or Y; and/or (d) a light chain variable region (VL) CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SQX₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅LX₁₇ (SEQ ID NO: 148), wherein X₁ is K or R; X₂ is A or S; X₅ is G or S; X₆ is I, L, or V; X₇ is L or S; X₈ is not present or H or Y; X₉ is not present or S; X₁₀ is not present or N or S; X₁₁ is not present or G or N; X₁₂ is not present or N; X₁₃ is not present or K or Y; X₁₄ is N, R, or S; X₁₅ is N, W, or Y; and X₁₇ is A or D; (e) a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SX₄X₅X₆X₇ (SEQ ID NO: 149), wherein X₁ is D, G, L, S, or W; X₂ is A or G; X₄ is N, S, or T; X₅ is L or R; X₆ is A, E, or Q; and X₇ is S or T; and/or (f) a VL CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁QX₃X₄X₅X₆PX₈T (SEQ ID NO: 150), wherein X₁ is M or Q; X₃ is F, G, H, I, R, or Y; X₄ is A, F, H, I, L, or Y; X₅ is A, G, H, S, T, V, or Y; X₆ is F, L, T, W, or Y; and X₈ is not present or F, L, P, or W.

In some embodiments, the VH CDR1 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 9-16. In some embodiments, the VH CDR2 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 25-32. In some embodiments, the VL CDR1 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 81-88. In some embodiments, the VL CDR2 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 97-104. In some embodiments, the VL CDR3 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 113-120.

In some embodiments, the binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 9; a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 25; a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 41; a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 81; a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 97; and a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 113; (b) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 10; a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 26; a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 42; a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 82; a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 98; and a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 114; (c) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 11; a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 27; a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 43; a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 83; a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 99; and a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 115; (d) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 12; a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 28; a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 44; a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 84; a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 100; and a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 116; (e) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 13; a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 29; a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 45; a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 85; a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 101; and a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 117; (f) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 14; a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 30; a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 46; a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 86; a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 102; and a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 118; (g) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 15; a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 31; a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 47; a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 87; a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 103; and a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 119; or (h) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 16; a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 32; a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 48; a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 88; a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 104; and a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 120.

In some embodiments, the binding molecule is single chained. In some embodiments, the binding molecule comprises an scFv.

In some embodiments, the CAR comprises a transmembrane domain. In some embodiments, the transmembrane domain is a transmembrane domain of CD28, 4-1BB/CD137, CD8 (e.g., CD8 alpha, CD4, CD19, CD3 epsilon, CD45, CD5, CD9, CD16, CD22, CD33, CD37, CD64, CD80, CD86, CD134, CD137, CD154, an alpha chain of a T cell receptor, a beta chain of a T cell receptor, a zeta chain of a T cell receptor, or any combination thereof. In some embodiments, the CAR comprises a hinge region between the transmembrane domain and the binding molecule. In some embodiments, the hinge region is of IgG1, IgG2, IgG3, IgG4, IgA, IgD, IgE, IgM, CD28, or CD8 alpha. In some embodiments, the CAR or TCR comprises a costimulatory region. In some embodiments, the costimulatory region is a signaling region of CD28, OX-40, 4-1BB/CD137, CD2, CD7, CD27, CD30, CD40, programmed death-1 (PD-1), inducible T cell costimulator (ICOS), lymphocyte function-associated antigen-1 (LFA-1 (CD11a/CD18), CD3 gamma, CD3 delta, CD3 epsilon, CD247, CD276 (B7-H3), LIGHT (tumor necrosis factor superfamily member 14; TNFSF14), NKG2C, Ig alpha (CD79a), DAP-10, Fc gamma receptor, MHC class I molecule, TNF receptor proteins, Immunoglobulin-like proteins, cytokine receptors, integrins, signaling lymphocytic activation molecules (SLAM proteins), activating NK cell receptors, BTLA, a Toll ligand receptor, ICAM-1, B7-H3, CDS, ICAM-1, GITR, BAFFR, LIGHT, HVEM (LIGHTR), KIRDS2, SLAMF7, NKp80 (KLRF1), NKp44, NKp30, NKp46, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, ITGAM, CD11b, ITGAX, CD11c, ITGB1, CD29, ITGB2, CD18, LFA-1, ITGB7, NKG2D, TNFR2, TRANCE/RANKL, DNAM1 (CD226), SLAMF4 (CD244, 2B4), CD84, CD96 (Tactile), CEACAM1, CRT AM, Ly9 (CD229), CD160 (BY55), PSGL1, CD100 (SEMA4D), CD69, SLAMF6 (NTB-A, Ly108), SLAM (SLAMF1, CD150, IPO-3), BLAME (SLAMF8), SELPLG (CD162), LTBR, LAT, GADS, SLP-76, PAG/Cbp, CD19a, a ligand that specifically binds with CD83, or any combination thereof. In some embodiments, the CAR or TCR comprises an activation domain. In some embodiments, the activation domain is a CD3 zeta domain.

In other embodiments, the invention is directed to a vector comprising the polynucleotide or a polypeptide encoded by the polynucleotide.

In certain embodiments, the invention is directed to a cell comprising the polynucleotide, the vector, the polypeptide, or any combination thereof. In other embodiments, the invention is directed to a cell, e.g., an immune cell, e.g., a tumor-infiltrating lymphocyte (TIL), autologous T cell, engineered autologous T cell (eACT), an allogeneic T cell, or any combination thereof.

In other embodiments, the invention is directed to a method of inducing an immunity against a tumor comprising administering to a subject an effective amount of a cell comprising the polynucleotide, the vector, the polypeptide, or any combination thereof. Other aspects of the invention include a method of treating a cancer in a subject in need thereof comprising administering to the subject the polynucleotide, the vector, the polypeptide, the cell, or the composition. The cancer treatable by the method can be a hematologic cancer.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1A-1F show CLUTSTAL W (1.83) multiple sequence alignments of eight example anti-BCMA binding molecules disclosed herein. FIG. 1A shows a sequence alignment of example anti-BCMA binding molecules comprising a VH domain. Complementarity determining regions (CDRs) and framework regions (FRs) are shown, as determined by Chothia. FIG. 1B is a table providing the SEQ ID NO for each VH, CDR, and FR sequence illustrated in FIG. 1A. FIG. 1C shows a sequence alignment of example anti-BCMA binding molecules comprising a VH domain, with alternate CDRs and FRs shown. FIG. 1D is a table providing the SEQ ID NO for each VH, CDR, and FR sequence illustrated in FIG. 1C. FIG. 1E shows a sequence alignment of example anti-BCMA binding molecules comprising a VL domain. CDRs and FRs are shown, as determined by Chothia. FIG. 1F is a table providing the SEQ ID NO for each VH, CDR, and FR sequence illustrated in FIG. 1E.

FIGS. 2A-2F show BCMA expression in various cells. FIG. 2A shows multiple myeloma cell expression of BCMA, CD138, CS-1, CD38, and CD19. Box-plot analysis shows the distribution of gene expression levels in the various multiple myeloma cell lines tested (FIG. 2A). FIGS. 2B-2D show BCMA expression in EoL1 (FIG. 2B), MM1S (FIG. 2C), and NCI-H929 (FIG. 2D) cancer cell lines as measured by flow cytometric analysis of BCMA cell surface expression on the respective cell lines. FIG. 2E shows the expression of BCMA, CS-1, CLL-1, DLL3, CD70, and FLT3 in alternatively activated macrophages; CD14-positive, CD16-negative cells; CD38-negative naïve B cells; CD4-positive, alpha-beta T cells; central memory CD4-positive cells; central memory CD8-positive cells; class switched memory B cells; cytotoxic CD56-dim natural killer cell; effector memory CD4-positive cells; effector memory CD8-positive cells; inflammatory macrophages; macrophages; mature neutrophils; memory B cells; monocytes; myeloid cells; and regulatory T cells. FIG. 2F shows the expression of BCMA, CD138, CS-1, CD38, and CD19 in the same cell types as in FIG. 2E. Gene expression is shown as fragments per kilobase of exon per million reads mapped (FPKM) (FIG. 2A, FIG. 2E, and FIG. 2F).

FIG. 3A and FIG. 3B show CAR expression in lentivirus transduced primary human T cells from a first healthy donor (FIG. 3A) and a second healthy donor (FIG. 3B).

FIGS. 4A-4F shows IFNγ, TNFα, and IL-2 production by lentivirus transduced CAR T cells from two healthy donors following 16 hours of co-cultured with EoL-1 (Black), NCI-H929 (light grey), or MM1S (grey) target cell lines. FIGS. 4A and 4B show the IFNγ (pg/ml; y-axis) production in lentivirus transduced CAR T cells from a first donor (FIG. 4A) and a second donor (FIG. 4B). FIGS. 4C and 4D show the TNFα (pg/ml; y-axis) production in lentivirus transduced CAR T cells from a first donor (FIG. 4C) and a second donor (FIG. 4D). FIGS. 4E and 4F show the IL-2 production (pg/ml; y-axis) in lentivirus transduced CAR T cells from a first donor (FIG. 4E) and a second donor (FIG. 4F).

FIGS. 5A-5F show the average cytolytic activity (as a percentage of viable target cells remaining; y-axis) over time from two healthy donors expressing the indicated CARs co-cultured with EoL1 (FIGS. 5A and 5B), NCI-H929 (FIGS. 5C and 5D), or MM1S (FIGS. 5E and 5F) target cells for 16 hours, 40 hours, 64 hours, 88 hours, or 112 hours. FIGS. 5A and 5B show the average cytolytic activity of transduced CART cells from a first donor (FIG. 5A) and a second donor (FIG. 5B) co-cultured with EoL1 target cells for 16 hours, 40 hours, 64 hours, 88 hours, or 112 hours. FIGS. 5C and 5D show the average cytolytic activity of transduced CAR T cells from a first donor (FIG. 5C) and a second donor (FIG. 5D) co-cultured with NCI-H929 target cells for 16 hours, 40 hours, 64 hours, 88 hours, or 112 hours. FIGS. 5E and 5F show the average cytolytic activity of transduced CART cells from a first donor (FIG. 5E) and a second donor (FIG. 5F) co-cultured with MM1S target cells for 16 hours, 40 hours, 64 hours, 88 hours, or 112 hours.

FIGS. 6A and 6B show proliferation of CFSE-labeled lentivirus transduced CART cells from a first healthy donor (FIG. 6A) and a second healthy donor (FIG. 6B) following 5 days of co-culture with CD3-CD28 beads (top row), EoL-1 (second row), NCI-H929 (third row), or MM1S (bottom row) target cell lines.

In the Figure descriptions below, underlined sequences denote CDR regions calculated using Chothia.

FIG. 7A shows Clone FS-26528 HC DNA sequence (SEQ ID NO: 271)

FIG. 7B shows Clone FS-26528 HC AA sequence (SEQ ID NO: 272)

FIG. 7C shows HC CDR sequences for clone FS-26528.

FIG. 7D shows Clone FS-26528 LC DNA sequence (SEQ ID NO: 276).

FIG. 7E shows Clone FS-26528 LC AA sequence (SEQ ID NO: 277).

FIG. 7F shows LC CDR sequences for clone FS-26528.

FIG. 7G shows Clone FS-26528 CAR DNA H×L sequences (SEQ ID NO: 281)

FIG. 7H shows Clone FS-26528 CAR H×L AA sequences (SEQ ID NO: 282)

FIG. 7I shows Clone FS-26528 CAR DNA L×H sequences (SEQ ID NO: 283).

FIG. 7J shows Clone FS-26528 CAR L×H sequences (SEQ ID NO: 284).

FIG. 8A shows Clone PC-26534 HC DNA sequence (SEQ ID NO: 285).

FIG. 8B shows Clone PC-26534 HC sequence (SEQ ID NO: 286).

FIG. 8C shows HC CDR sequences for clone FS-26528.

FIG. 8D shows Clone PC-26534 LC DNA sequences (SEQ ID NO: 290).

FIG. 8E shows the Clone PC-26534 LC sequence (SEQ ID NO: 291).

FIG. 8F shows LC CDR sequences for Clone PC-26534.

FIG. 8G shows the Clone PC-26534 CAR DNA H×L sequence (SEQ ID NO: 295).

FIG. 8H shows the Clone PC-26534 CAR H×L AA sequence (SEQ ID NO: 296)

FIG. 8I shows the Clone PC-26534 CAR DNA L×H sequence (SEQ ID NO: 297).

FIG. 8J shows Clone PC-26534 CAR L×H sequence (SEQ ID NO: 298).

FIG. 9A shows Clone AJ-26545 HC DNA sequence (SEQ ID NO: 299).

FIG. 9B shows Clone AJ-26545 variable HC sequence (SEQ ID NO: 300).

FIG. 9C shows HC CDR sequences for Clone AJ-26545.

FIG. 9D shows Clone AJ-26545 variable LC DNA sequence (SEQ ID NO: 304).

FIG. 9E shows Clone AJ-26545 variable LC AA sequence (SEQ ID NO: 305)

FIG. 9F shows Clone AJ-26545 LC CDR sequences.

FIG. 9G shows Clone AJ-26545 CAR DNA H×L sequence (SEQ ID NO: 309).

FIG. 9H shows Clone AJ-26545 CAR H×L AA sequence (SEQ ID NO: 310)

FIG. 9I shows Clone AJ-26545 CAR DNA L×H sequence (SEQ ID NO: 311)

FIG. 9J shows Clone AJ-26545 CAR L×H sequence (SEQ ID NO: 312).

FIG. 10A shows Clone AJ-26554 HC DNA sequence (SEQ ID NO: 313)

FIG. 10B shows Clone AJ-26554 HC AA sequence (SEQ ID NO: 314).

FIG. 10C shows Clone AJ-26554 HC CDR sequences

FIG. 10D shows Clone AJ-26554 LC DNA sequence (SEQ ID NO: 318).

FIG. 10E shows Clone AJ-26554 LC AA sequence (SEQ ID NO: 319).

FIG. 10F shows Clone AJ-26554 LC CDR sequences.

FIG. 10G shows Clone AJ-26554 CAR DNA H×L chain sequences (SEQ ID NO: 323).

FIG. 10H shows Clone AJ-26554 CAR H×L chain AA sequences (SEQ ID NO: 324).

FIG. 10I shows Clone AJ-26554 CAR DNA L×H chain sequences (SEQ ID NO: 325).

FIG. 10J shows Clone AJ-26554 CAR L×H AA sequences (SEQ ID NO: 326).

FIG. 11A shows Clone NM-26562 HC DNA sequence (SEQ ID NO: 327).

FIG. 11B shows Clone NM-26562 HC AA sequence (SEQ ID NO: 328).

FIG. 11C shows Clone NM-26562 HC CDR sequences.

FIG. 11D shows Clone NM-26562 LC DNA sequence (SEQ ID NO: 332).

FIG. 11E shows Clone NM-26562 LC AA sequence (SEQ ID NO: 333).

FIG. 11F shows the Clone NM-26562 LC CDR sequences.

FIG. 11G shows the Clone NM-26562 CAR DNA H×L sequences (SEQ ID NO: 337)

FIG. 11H shows Clone NM-26562 CAR H×L AA sequences (SEQ ID NO: 338).

FIG. 11I shows Clone NM-26562 CAR DNA L×H sequences (SEQ ID NO: 339).

FIG. 11J shows Clone NM-26562 CAR L×H AA sequences (SEQ ID NO: 340).

FIG. 12A shows Clone TS-26564 HC DNA sequence (SEQ ID NO: 341).

FIG. 12B shows Clone TS-26564 HC AA sequence (SEQ ID NO: 342).

FIG. 12C shows the Clone TS-26564 HC CDR sequences.

FIG. 12D shows the Clone TS-26564 LC DNA sequence (SEQ ID NO: 346).

FIG. 12E shows the Clone TS-26564 LC AA sequence (SEQ ID NO: 347).

FIG. 12F shows the Clone TS-26564 LC CDR sequences.

FIG. 12G shows the Clone TS-26564 CAR DNA H×L sequences (SEQ ID NO: 351).

FIG. 12H shows the Clone TS-26564 CAR H×L chain AA sequences (SEQ ID NO: 352).

FIG. 12I shows the Clone TS-26564 CAR DNA L×H sequences (SEQ ID NO: 353)

FIG. 12J shows the Clone TS-26564 CAR L×H AA sequences (SEQ ID NO: 354)

FIG. 13A shows the Clone RY-26568 HC DNA sequence (SEQ ID NO: 355)

FIG. 13B shows the Clone RY-26568 HC AA sequence (SEQ ID NO: 356).

FIG. 13C shows the Clone RY-26568 HC CDR sequences.

FIG. 13D shows the Clone RY-26568 LC DNA sequence (SEQ ID NO: 360).

FIG. 13E shows the Clone RY-26568 LC AA sequence (SEQ ID NO: 361).

FIG. 13F shows the Clone RY-26568 LC CDR AA sequences.

FIG. 13G shows the Clone RY-26568 CAR DNA H×L sequences (SEQ ID NO: 365)

FIG. 13H shows the Clone RY-26568 CAR H×L AA sequences (SEQ ID NO: 366).

FIG. 13I shows the Clone RY-26568 CAR DNA L×H sequences (SEQ ID NO: 367).

FIG. 13J shows the Clone RY-26568 CAR L×H AA sequences (SEQ ID NO: 368).

FIG. 14A shows the Clone PP-26575 HC DNA sequence (SEQ ID NO: 369).

FIG. 14B shows the Clone PP-26575 HC AA sequence (SEQ ID NO: 370).

FIG. 14C shows the Clone PP-26575 HC CDR AA sequences.

FIG. 14D shows the Clone PP-26575 LC DNA sequence (SEQ ID NO: 374).

FIG. 14E shows the Clone PP-26575 LC AA sequence (SEQ ID NO: 375).

FIG. 14F shows the Clone PP-26575 LC CDR AA sequences.

FIG. 14G shows the Clone PP-26575 CAR DNA H×L sequences (SEQ ID NO: 379).

FIG. 14H shows Clone PP-26575 CAR H×L AA sequences (SEQ ID NO: 380).

FIG. 14I shows Clone PP-26575 CAR DNA L×H sequence (SEQ ID NO: 381).

FIG. 14J shows the Clone PP-26575 CAR L×H AA sequence (SEQ ID NO: 382).

FIG. 15A shows the Clone RD-26576 HC DNA sequence (SEQ ID NO: 383)

FIG. 15B shows Clone RD-26576 HC AA sequence (SEQ ID NO: 384).

FIG. 15C shows the Clone RD-26576 HC CDR sequences.

FIG. 15D shows the Clone RD-26576 LC DNA sequence (SEQ ID NO: 388)

FIG. 15E shows the Clone RD-26576 LC AA sequence (SEQ ID NO: 389).

FIG. 15F shows the Clone RD-26576 LC CDR sequences.

FIG. 15G shoes the Clone RD-26576 CAR DNA H×L sequences (SEQ ID NO: 393).

FIG. 15H shows the Clone RD-26576 CAR H×L chain AA sequences (SEQ ID NO: 394).

FIG. 15I shows the Clone RD-26576 CAR DNA L×H sequences (SEQ ID NO: 395).

FIG. 15J shows the Clone RD-26576 CAR L×H AA sequences (SEQ ID NO: 396).

FIG. 16A shows the Clone RD-26578 HC DNA sequences (SEQ ID NO: 397).

FIG. 16B shows the Clone RD-26578 HC AA sequence (SEQ ID NO: 398).

FIG. 16C shows the Clone RD-26578 HC CDR AA sequences.

FIG. 16D shows the Clone RD-26578 LC DNA sequence (SEQ ID NO: 402).

FIG. 16E shows the Clone RD-26578 LC AA sequence (SEQ ID NO: 403)

FIG. 16F shows the Clone RD-26578 LC CDR sequences.

FIG. 16G shows the Clone RD-26578 CAR DNA H×L chain sequence (SEQ ID NO: 407).

FIG. 16H shows the Clone RD-26578 CAR H×L AA sequence (SEQ ID NO: 408).

FIG. 16I shows the Clone RD-26578 CAR DNA L×H sequences (SEQ ID NO: 409).

FIG. 16J shows the Clone RD-26578 CAR L×H AA sequence (SEQ ID NO: 410).

FIG. 17 shows the outcome of an in vivo study examining the efficacy of clone RD-21530 in a subcutaneous RPMI-8226 mouse model. Cohorts of 10 mice each were tested for the CAR (dashed lines) and mock transduced (bolded lines) T cells.

FIG. 18A and FIG. 18B show the outcome of an in vitro cytotoxicity assay using the optimized BCMA scFv variants cocultured with NCI-H929 and MM.1S cells, respectively. CAR T cells using these optimized scFvs were incubated overnight with luciferase labeled target cells in 3:1 and 1:1 effector to target cell ratios.

FIG. 19 shows the pGAR vector map.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to antibodies, antigen binding molecules thereof, chimeric antigen receptors (CARs), and engineered T cell receptors, which bind BCMA, polynucleotides encoding the same, and in vitro cells comprising the same. The polynucleotides, polypeptides, and in vitro cells described herein can be used in an engineered CAR T cell therapy, e.g., an autologous cell therapy (eACT™), for the treatment of a patient suffering from a cancer. In particular, the polynucleotides, polypeptides, and in vitro cells described herein can be used for the treatment of multiple myeloma.

I. Definitions

In order that the present disclosure may be more readily understood, certain terms are first defined. As used in this application, except as otherwise expressly provided herein, each of the following terms shall have the meaning set forth below. Additional definitions are set forth throughout the application.

The term “and/or” where used herein is to be taken as specific disclosure of each of the two specified features or components with or without the other. Thus, the term “and/or” as used in a phrase such as “A and/or B” herein is intended to include “A and B,” “A or B,” “A” (alone), and “B” (alone). Likewise, the term “and/or” as used in a phrase such as “A, B, and/or C” is intended to encompass each of the following aspects: A, B, and C; A, B, or C; A or C; A or B; B or C; A and C; A and B; B and C; A (alone); B (alone); and C (alone).

It is understood that wherever aspects are described herein with the language “comprising,” otherwise analogous aspects described in terms of “consisting of” and/or “consisting essentially of” are also provided.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure is related. For example, the Concise Dictionary of Biomedicine and Molecular Biology, Juo, Pei-Show, 2nd ed., 2002, CRC Press; The Dictionary of Cell and Molecular Biology, 3rd ed., 1999, Academic Press; and the Oxford Dictionary Of Biochemistry And Molecular Biology, Revised, 2000, Oxford University Press, provide one of skill with a general dictionary of many of the terms used in this disclosure.

Units, prefixes, and symbols are denoted in their Système International de Unites (SI) accepted form. Numeric ranges are inclusive of the numbers defining the range. The headings provided herein are not limitations of the various aspects of the disclosure, which can be had by reference to the specification as a whole. Accordingly, the terms defined immediately below are more fully defined by reference to the specification in its entirety.

“Administering” refers to the physical introduction of an agent to a subject, using any of the various methods and delivery systems known to those skilled in the art. Exemplary routes of administration for the formulations disclosed herein include intravenous, intramuscular, subcutaneous, intraperitoneal, spinal or other parenteral routes of administration, for example by injection or infusion. The phrase “parenteral administration” as used herein means modes of administration other than enteral and topical administration, usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intralymphatic, intralesional, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intraarticular, subcapsular, subarachnoid, intraspinal, epidural and intrasternal injection and infusion, as well as in vivo electroporation. In some embodiments, the formulation is administered via a non-parenteral route, e.g., orally. Other non-parenteral routes include a topical, epidermal or mucosal route of administration, for example, intranasally, vaginally, rectally, sublingually or topically. Administering can also be performed, for example, once, a plurality of times, and/or over one or more extended periods.

The term “antibody” (Ab) includes, without limitation, a glycoprotein immunoglobulin which binds specifically to an antigen. In general, and antibody can comprise at least two heavy (H) chains and two light (L) chains interconnected by disulfide bonds, or an antigen binding molecule thereof. Each H chain comprises a heavy chain variable region (abbreviated herein as VH) and a heavy chain constant region. The heavy chain constant region comprises three constant domains, CH1, CH2 and CH3. Each light chain comprises a light chain variable region (abbreviated herein as VL) and a light chain constant region. The light chain constant region is comprises one constant domain, CL. The VH and VL regions can be further subdivided into regions of hypervariability, termed complementarity determining regions (CDRs), interspersed with regions that are more conserved, termed framework regions (FR). Each VH and VL comprises three CDRs and four FRs, arranged from amino-terminus to carboxy-terminus in the following order: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4. The variable regions of the heavy and light chains contain a binding domain that interacts with an antigen. The constant regions of the Abs may mediate the binding of the immunoglobulin to host tissues or factors, including various cells of the immune system (e.g., effector cells) and the first component (C1q) of the classical complement system.

Antibodies can include, for example, monoclonal antibodies, recombinantly produced antibodies, monospecific antibodies, multispecific antibodies (including bispecific antibodies), human antibodies, humanized antibodies, chimeric antibodies, immunoglobulins, synthetic antibodies, tetrameric antibodies comprising two heavy chain and two light chain molecules, an antibody light chain monomer, an antibody heavy chain monomer, an antibody light chain dimer, an antibody heavy chain dimer, an antibody light chain-antibody heavy chain pair, intrabodies, antibody fusions (sometimes referred to herein as “antibody conjugates”), heteroconjugate antibodies, single domain antibodies, monovalent antibodies, single chain antibodies or single-chain Fvs (scFv), camelized antibodies, affybodies, Fab fragments, F(ab′)₂ fragments, disulfide-linked Fvs (sdFv), anti-idiotypic (anti-Id) antibodies (including, e.g., anti-anti-Id antibodies), minibodies, domain antibodies, synthetic antibodies (sometimes referred to herein as “antibody mimetics”), and antigen-binding fragments of any of the above. In certain embodiments, antibodies described herein refer to polyclonal antibody populations.

An immunoglobulin may derive from any of the commonly known isotypes, including but not limited to IgA, secretory IgA, IgG and IgM. IgG subclasses are also well known to those in the art and include but are not limited to human IgG1, IgG2, IgG3 and IgG4. “Isotype” refers to the Ab class or subclass (e.g., IgM or IgG1) that is encoded by the heavy chain constant region genes. The term “antibody” includes, by way of example, both naturally occurring and non-naturally occurring Abs; monoclonal and polyclonal Abs; chimeric and humanized Abs; human or nonhuman Abs; wholly synthetic Abs; and single chain Abs. A nonhuman Ab may be humanized by recombinant methods to reduce its immunogenicity in man. Where not expressly stated, and unless the context indicates otherwise, the term “antibody” also includes an antigen-binding fragment or an antigen binding molecule of any of the aforementioned immunoglobulins, and includes a monovalent and a divalent fragment or portion, and a single chain Ab.

An “antigen binding molecule,” “antigen binding portion,” or “antibody fragment” refers to any molecule that comprises the antigen binding parts (e.g., CDRs) of the antibody from which the molecule is derived. An antigen binding molecule can include the antigenic complementarity determining regions (CDRs). Examples of antibody fragments include, but are not limited to, Fab, Fab′, F(ab′)2, and Fv fragments, dAb, linear antibodies, scFv antibodies, and multispecific antibodies formed from antigen binding molecules. Peptibodies (i.e., Fc fusion molecules comprising peptide binding domains) are another example of suitable antigen binding molecules. In some embodiments, the antigen binding molecule binds to an antigen on a tumor cell. In some embodiments, the antigen binding molecule binds to an antigen on a cell involved in a hyperproliferative disease or to a viral or bacterial antigen. In certain embodiments, the antigen binding molecule binds to BCMA. In further embodiments, the antigen binding molecule is an antibody of fragment thereof, including one or more of the complementarity determining regions (CDRs) thereof. In further embodiments, the antigen binding molecule is a single chain variable fragment (scFv). In some embodiments, the antigen binding molecule comprises or consists of avimers.

As used herein, the terms “variable region” or “variable domain” are used interchangeably and are common in the art. The variable region typically refers to a portion of an antibody, generally, a portion of a light or heavy chain, typically about the amino-terminal 110 to 120 amino acids in the mature heavy chain and about 90 to 115 amino acids in the mature light chain, which differ extensively in sequence among antibodies and are used in the binding and specificity of a particular antibody for its particular antigen. The variability in sequence is concentrated in those regions called complementarity determining regions (CDRs) while the more highly conserved regions in the variable domain are called framework regions (FR). Without wishing to be bound by any particular mechanism or theory, it is believed that the CDRs of the light and heavy chains are primarily responsible for the interaction and specificity of the antibody with antigen. In certain embodiments, the variable region is a human variable region. In certain embodiments, the variable region comprises rodent or murine CDRs and human framework regions (FRs). In particular embodiments, the variable region is a primate (e.g., non-human primate) variable region. In certain embodiments, the variable region comprises rodent or murine CDRs and primate (e.g., non-human primate) framework regions (FRs).

The terms “VL” and “VL domain” are used interchangeably to refer to the light chain variable region of an antibody or an antigen-binding fragment thereof.

The terms “VH” and “VH domain” are used interchangeably to refer to the heavy chain variable region of an antibody or an antigen-binding fragment thereof.

A number of definitions of the CDRs are commonly in use: Kabat numbering, Chothia numbering, AbM numbering, or contact numbering. The AbM definition is a compromise between the two used by Oxford Molecular's AbM antibody modelling software. The contact definition is based on an analysis of the available complex crystal structures.

TABLE 1 CDR Numbering Loop Kabat AbM Chothia Contact L1 L24 - - - L34 L24 - - - L34 L24 - - - L34 L30 - - - L36 L2 L50 - - - L56 L50 - - - L56 L50 - - - L56 L46 - - - L55 L3 L89 - - - L97 L89 - - - L97 L89 - - - L97 L89 - - - L96 H1 H31 - - - H35B H26 - - - H35B H26 - - - H32 . . . 34 H30 - - - H35B (Kabat Numbering) H1 H31 - - - H35 H26 - - - H35 H26 - - - H32 H30 - - - H35 (Chothia Numbering) H2 H50 - - - H65 H50 - - - H58 H52 - - - H56 H47 - - - H58 H3 H95 - - - H102 H95 - - - H102 H95 - - - H102 H93 - - - H101

The term “Kabat numbering” and like terms are recognized in the art and refer to a system of numbering amino acid residues in the heavy and light chain variable regions of an antibody, or an antigen binding molecule thereof. In certain aspects, the CDRs of an antibody can be determined according to the Kabat numbering system (see, e.g., Kabat EA & Wu TT (1971) Ann NY Acad Sci 190: 382-391 and Kabat E A et al., (1991) Sequences of Proteins of Immunological Interest, Fifth Edition, U.S. Department of Health and Human Services, NIH Publication No. 91-3242). Using the Kabat numbering system, CDRs within an antibody heavy chain molecule are typically present at amino acid positions 31 to 35, which optionally can include one or two additional amino acids, following 35 (referred to in the Kabat numbering scheme as 35A and 35B) (CDR1), amino acid positions 50 to 65 (CDR2), and amino acid positions 95 to 102 (CDR3). Using the Kabat numbering system, CDRs within an antibody light chain molecule are typically present at amino acid positions 24 to 34 (CDR1), amino acid positions 50 to 56 (CDR2), and amino acid positions 89 to 97 (CDR3). In a specific embodiment, the CDRs of the antibodies described herein have been determined according to the Kabat numbering scheme.

In certain aspects, the CDRs of an antibody can be determined according to the Chothia numbering scheme, which refers to the location of immunoglobulin structural loops (see, e.g., Chothia C & Lesk AM, (1987), J Mol Biol 196: 901-917; Al-Lazikani B et al., (1997) J Mol Biol 273: 927-948; Chothia C et al., (1992) J Mol Biol 227: 799-817; Tramontano A et al., (1990) J Mol Biol 215(1): 175-82; and U.S. Pat. No. 7,709,226). Typically, when using the Kabat numbering convention, the Chothia CDR-H1 loop is present at heavy chain amino acids 26 to 32, 33, or 34, the Chothia CDR-H2 loop is present at heavy chain amino acids 52 to 56, and the Chothia CDR-H3 loop is present at heavy chain amino acids 95 to 102, while the Chothia CDR-L1 loop is present at light chain amino acids 24 to 34, the Chothia CDR-L2 loop is present at light chain amino acids 50 to 56, and the Chothia CDR-L3 loop is present at light chain amino acids 89 to 97. The end of the Chothia CDR-HI loop when numbered using the Kabat numbering convention varies between H32 and H34 depending on the length of the loop (this is because the Kabat numbering scheme places the insertions at H35A and H35B; if neither 35A nor 35B is present, the loop ends at 32; if only 35A is present, the loop ends at 33; if both 35A and 35B are present, the loop ends at 34). In a specific embodiment, the CDRs of the antibodies described herein have been determined according to the Chothia numbering scheme.

As used herein, the terms “constant region” and “constant domain” are interchangeable and have a meaning common in the art. The constant region is an antibody portion, e.g., a carboxyl terminal portion of a light and/or heavy chain which is not directly involved in binding of an antibody to antigen but which can exhibit various effector functions, such as interaction with the Fc receptor. The constant region of an immunoglobulin molecule generally has a more conserved amino acid sequence relative to an immunoglobulin variable domain.

As used herein, the term “heavy chain” when used in reference to an antibody can refer to any distinct type, e.g., alpha (α), delta (δ), epsilon (ε), gamma (γ) and mu (μ), based on the amino acid sequence of the constant domain, which give rise to IgA, IgD, IgE, IgG and IgM classes of antibodies, respectively, including subclasses of IgG, e.g., IgG₁, IgG₂, IgG₃ and IgG₄.

As used herein, the term “light chain” when used in reference to an antibody can refer to any distinct type, e.g., kappa (κ) or lambda (λ) based on the amino acid sequence of the constant domains. Light chain amino acid sequences are well known in the art. In specific embodiments, the light chain is a human light chain.

“Binding affinity” generally refers to the strength of the sum total of non-covalent interactions between a single binding site of a molecule (e.g., an antibody) and its binding partner (e.g., an antigen). Unless indicated otherwise, as used herein, “binding affinity” refers to intrinsic binding affinity which reflects a 1:1 interaction between members of a binding pair (e.g., antibody and antigen). The affinity of a molecule X for its partner Y can generally be represented by the dissociation constant (K_(D)). Affinity can be measured and/or expressed in a number of ways known in the art, including, but not limited to, equilibrium dissociation constant (K_(D)), and equilibrium association constant (K_(A)). The K_(D) is calculated from the quotient of k_(off)/k_(on), whereas K_(A) is calculated from the quotient of k_(on)/k_(off). k_(on) refers to the association rate constant of, e.g., an antibody to an antigen, and k_(off) refers to the dissociation of, e.g., an antibody to an antigen. The k_(on) and k_(off) can be determined by techniques known to one of ordinary skill in the art, such as BIAcore® or KinExA.

As used herein, a “conservative amino acid substitution” is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having side chains have been defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine, tryptophan), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). In certain embodiments, one or more amino acid residues within a CDR(s) or within a framework region(s) of an antibody or antigen-binding fragment thereof can be replaced with an amino acid residue with a similar side chain.

As used herein, an “epitope” is a term in the art and refers to a localized region of an antigen to which an antibody can specifically bind. An epitope can be, for example, contiguous amino acids of a polypeptide (linear or contiguous epitope) or an epitope can, for example, come together from two or more non-contiguous regions of a polypeptide or polypeptides (conformational, non-linear, discontinuous, or non-contiguous epitope). In certain embodiments, the epitope to which an antibody binds can be determined by, e.g., NMR spectroscopy, X-ray diffraction crystallography studies, ELISA assays, hydrogen/deuterium exchange coupled with mass spectrometry (e.g., liquid chromatography electrospray mass spectrometry), array-based oligo-peptide scanning assays, and/or mutagenesis mapping (e.g., site-directed mutagenesis mapping). For X-ray crystallography, crystallization may be accomplished using any of the known methods in the art (e.g., Giegé R et al., (1994) Acta Crystallogr D Biol Crystallogr 50(Pt 4): 339-350; McPherson A (1990) Eur J Biochem 189: 1-23; Chayen N E (1997) Structure 5: 1269-1274; McPherson A (1976) J Biol Chem 251: 6300-6303). Antibody:antigen crystals may be studied using well known X-ray diffraction techniques and may be refined using computer software such as X-PLOR (Yale University, 1992, distributed by Molecular Simulations, Inc.; see e.g. Meth Enzymol (1985) volumes 114 & 115, eds Wyckoff H W et al.; U.S. 2004/0014194), and BUSTER (Bricogne G (1993) Acta Crystallogr D Biol Crystallogr 49(Pt 1): 37-60; Bricogne G (1997) Meth Enzymol 276A: 361-423, ed Carter C W; Roversi P et al., (2000) Acta Crystallogr D Biol Crystallogr 56(Pt 10): 1316-1323). Mutagenesis mapping studies may be accomplished using any method known to one of skill in the art. See, e.g., Champe M et al., (1995) J Biol Chem 270: 1388-1394 and Cunningham B C & Wells J A (1989) Science 244: 1081-1085 for a description of mutagenesis techniques, including alanine scanning mutagenesis techniques.

As used herein, an antigen binding molecule, an antibody, or an antigen binding molecule thereof “cross competes” with a reference antibody or an antigen binding molecule thereof if the interaction between an antigen and the first binding molecule, an antibody, or an antigen binding molecule thereof blocks, limits, inhibits, or otherwise reduces the ability of the reference binding molecule, reference antibody, or an antigen binding molecule thereof to interact with the antigen. Cross competition can be complete, e.g., binding of the binding molecule to the antigen completely blocks the ability of the reference binding molecule to bind the antigen, or it can be partial, e.g., binding of the binding molecule to the antigen reduces the ability of the reference binding molecule to bind the antigen. In certain embodiments, an antigen binding molecule that cross competes with a reference antigen binding molecule binds the same or an overlapping epitope as the reference antigen binding molecule. In other embodiments, the antigen binding molecule that cross competes with a reference antigen binding molecule binds a different epitope as the reference antigen binding molecule. Numerous types of competitive binding assays can be used to determine if one antigen binding molecule competes with another, for example: solid phase direct or indirect radioimmunoassay (RIA); solid phase direct or indirect enzyme immunoassay (EIA); sandwich competition assay (Stahli et al., 1983, Methods in Enzymology 9:242-253); solid phase direct biotin-avidin EIA (Kirkland et al., 1986, J. Immunol. 137:3614-3619); solid phase direct labeled assay, solid phase direct labeled sandwich assay (Harlow and Lane, 1988, Antibodies, A Laboratory Manual, Cold Spring Harbor Press); solid phase direct label RIA using 1-125 label (Morel et al., 1988, Molec. Immunol. 25:7-15); solid phase direct biotin-avidin EIA (Cheung, et al., 1990, Virology 176:546-552); and direct labeled RIA (Moldenhauer et al., 1990, Scand. J. Immunol. 32:77-82).

As used herein, the terms “immunospecifically binds,” “immunospecifically recognizes,” “specifically binds,” and “specifically recognizes” are analogous terms in the context of antibodies and refer to molecules that bind to an antigen (e.g., epitope or immune complex) as such binding is understood by one skilled in the art. For example, a molecule that specifically binds to an antigen may bind to other peptides or polypeptides, generally with lower affinity as determined by, e.g., immunoassays, BIAcore®, KinExA 3000 instrument (Sapidyne Instruments, Boise, Id.), or other assays known in the art. In a specific embodiment, molecules that specifically bind to an antigen bind to the antigen with a K_(A) that is at least 2 logs, 2.5 logs, 3 logs, 4 logs or greater than the K_(A) when the molecules bind to another antigen.

In another embodiment, specific embodiment, molecules that specifically bind to an antigen bind with a dissociation constant (K_(d)) of about 1×10⁻⁷ M. In some embodiments, the antigen binding molecule specifically binds an antigen with “high affinity” when the K_(d) is about 1×10⁻⁹ M to about 5×10⁻⁹ M. In some embodiments, the antigen binding molecule specifically binds an antigen with “very high affinity” when the K_(d) is 1×10⁻¹⁰ M to about 5×10⁻¹⁰ M. In one embodiment, the antigen binding molecule has a K_(d) of 10⁻⁹ M. In one embodiment, the off-rate is less than about 1×10⁻⁵. In other embodiments, the antigen binding molecule binds human BCMA with a K_(d) of between about 1×10⁻⁷ M and about 1×10⁻¹³ M. In yet another embodiment, the antigen binding molecule binds human BCMA with a K_(d) of about 1×10⁻¹⁰ M to about 5×10⁻¹⁰ M.

In another specific embodiment, molecules that specifically bind to an antigen do not cross react with other proteins under similar binding conditions. In another specific embodiment, molecules that specifically bind to an antigen do not cross react with other non-BCMA proteins. In a specific embodiment, provided herein is an antibody or fragment thereof that binds to BCMA with higher affinity than to another unrelated antigen. In certain embodiments, provided herein is an antibody or fragment thereof that binds to BCMA (e.g., human BCMA) with a 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or higher affinity than to another, unrelated antigen as measured by, e.g., a radioimmunoassay, surface plasmon resonance, or kinetic exclusion assay. In a specific embodiment, the extent of binding of an anti-BCMA antibody or antigen-binding fragment thereof described herein to an unrelated, non-BCMA protein is less than 10%, 15%, or 20% of the binding of the antibody to BCMA protein as measured by, e.g., a radioimmunoassay.

In a specific embodiment, provided herein is an antibody or fragment thereof that binds to human BCMA with higher affinity than to another species of BCMA. In certain embodiments, provided herein is an antibody or fragment thereof that binds to human BCMA with a 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70% or higher affinity than to another species of BCMA as measured by, e.g., a radioimmunoassay, surface plasmon resonance, or kinetic exclusion assay. In a specific embodiment, an antibody or fragment thereof described herein, which binds to human BCMA, will bind to another species of BCMA protein with less than 10%, 15%, or 20% of the binding of the antibody or fragment thereof to the human BCMA protein as measured by, e.g., a radioimmunoassay, surface plasmon resonance, or kinetic exclusion assay.

An “antigen” refers to any molecule that provokes an immune response or is capable of being bound by an antibody or an antigen binding molecule. The immune response may involve either antibody production, or the activation of specific immunologically-competent cells, or both. A person of skill in the art would readily understand that any macromolecule, including virtually all proteins or peptides, can serve as an antigen. An antigen can be endogenously expressed, i.e. expressed by genomic DNA, or can be recombinantly expressed. An antigen can be specific to a certain tissue, such as a cancer cell, or it can be broadly expressed. In addition, fragments of larger molecules can act as antigens. In one embodiment, antigens are tumor antigens. In one particular embodiment, the antigen is BCMA.

The term “neutralizing” refers to an antigen binding molecule, scFv, antibody, or a fragment thereof that binds to a ligand and prevents or reduces the biological effect of that ligand. In some embodiments, the antigen binding molecule, scFv, antibody, or a fragment thereof, directly blocking a binding site on the ligand or otherwise alters the ligand's ability to bind through indirect means (such as structural or energetic alterations in the ligand). In some embodiments, the antigen binding molecule, scFv, antibody, or a fragment thereof prevents the protein to which it is bound from performing a biological function.

As used herein, the term “BCMA” refers to B cell maturation antigen, which can include, but is not limited to, native BCMA, an isoform of BCMA, or an interspecies BCMA homolog of BCMA. BCMA (also known as TNFRSF17, CD269, and TNFRSF13A) is a member of the tumor necrosis factor (TNF)-receptor superfamily. BCMA is expressed on the surface of multiple myeloma cells, while highly restricted to plasma cells and a subset of mature B cells in healthy tissue (FIG. 2A and FIG. 2C). The amino acid sequence of human BCMA (hBCMA) is provided in NCBI Accession Q02223.2 (GI:313104029) (SEQ ID NO: 163). As used herein, BCMA includes human BCMA and non-human BCMA homologs, as well as variants, fragments, or post-transnationally modified forms thereof, including, but not limited to, N- and O-linked glycosylated forms of BCMA. BCMA proteins may further include fragments comprising all or a portion of the extracellular domain of BCMA (e.g., all or a portion of amino acids 1-54 of hBCMA).

The term “autologous” refers to any material derived from the same individual to which it is later to be re-introduced. For example, the engineered autologous cell therapy (eACT™) method described herein involves collection of lymphocytes from a patient, which are then engineered to express, e.g., a CAR construct, and then administered back to the same patient.

The term “allogeneic” refers to any material derived from one individual which is then introduced to another individual of the same species, e.g., allogeneic T cell transplantation.

The terms “transduction” and “transduced” refer to the process whereby foreign DNA is introduced into a cell via viral vector (see Jones et al., “Genetics: principles and analysis,” Boston: Jones & Bartlett Publ. (1998)). In some embodiments, the vector is a retroviral vector, a DNA vector, a RNA vector, an adenoviral vector, a baculoviral vector, an Epstein Barr viral vector, a papovaviral vector, a vaccinia viral vector, a herpes simplex viral vector, an adenovirus associated vector, a lentiviral vector, or any combination thereof.

A “cancer” refers to a broad group of various diseases characterized by the uncontrolled growth of abnormal cells in the body. Unregulated cell division and growth results in the formation of malignant tumors that invade neighboring tissues and may also metastasize to distant parts of the body through the lymphatic system or bloodstream. A “cancer” or “cancer tissue” can include a tumor. Examples of cancers that can be treated by the methods of the present invention include, but are not limited to, cancers of the immune system including lymphoma, leukemia, myeloma, and other leukocyte malignancies. In some embodiments, the methods of the present invention can be used to reduce the tumor size of a tumor derived from, for example, bone cancer, pancreatic cancer, skin cancer, cancer of the head or neck, cutaneous or intraocular malignant melanoma, uterine cancer, ovarian cancer, rectal cancer, cancer of the anal region, stomach cancer, testicular cancer, uterine cancer, carcinoma of the fallopian tubes, carcinoma of the endometrium, carcinoma of the cervix, carcinoma of the vagina, carcinoma of the vulva, multiple myeloma, Hodgkin's Disease, non-Hodgkin's lymphoma (NHL), primary mediastinal large B cell lymphoma (PMBC), diffuse large B cell lymphoma (DLBCL), follicular lymphoma (FL), transformed follicular lymphoma, splenic marginal zone lymphoma (SMZL), cancer of the esophagus, cancer of the small intestine, cancer of the endocrine system, cancer of the thyroid gland, cancer of the parathyroid gland, cancer of the adrenal gland, sarcoma of soft tissue, cancer of the urethra, cancer of the penis, chronic or acute leukemia, acute myeloid leukemia, chronic myeloid leukemia, acute lymphoblastic leukemia (ALL) (including non T cell ALL), chronic lymphocytic leukemia (CLL), solid tumors of childhood, lymphocytic lymphoma, cancer of the bladder, cancer of the kidney or ureter, carcinoma of the renal pelvis, neoplasm of the central nervous system (CNS), primary CNS lymphoma, tumor angiogenesis, spinal axis tumor, brain stem glioma, pituitary adenoma, Kaposi's sarcoma, epidermoid cancer, squamous cell cancer, T-cell lymphoma, environmentally induced cancers including those induced by asbestos, other B cell malignancies, and combinations of said cancers. In one particular embodiment, the cancer is multiple myeloma. The particular cancer can be responsive to chemo- or radiation therapy or the cancer can be refractory. A refractor cancer refers to a cancer that is not amendable to surgical intervention and the cancer is either initially unresponsive to chemo- or radiation therapy or the cancer becomes unresponsive over time.

An “anti-tumor effect” as used herein, refers to a biological effect that can present as a decrease in tumor volume, a decrease in the number of tumor cells, a decrease in tumor cell proliferation, a decrease in the number of metastases, an increase in overall or progression-free survival, an increase in life expectancy, or amelioration of various physiological symptoms associated with the tumor. An anti-tumor effect can also refer to the prevention of the occurrence of a tumor, e.g., a vaccine.

A “cytokine,” as used herein, refers to a non-antibody protein that is released by one cell in response to contact with a specific antigen, wherein the cytokine interacts with a second cell to mediate a response in the second cell. A cytokine can be endogenously expressed by a cell or administered to a subject. Cytokines may be released by immune cells, including macrophages, B cells, T cells, and mast cells to propagate an immune response. Cytokines can induce various responses in the recipient cell. Cytokines can include homeostatic cytokines, chemokines, pro-inflammatory cytokines, effectors, and acute-phase proteins. For example, homeostatic cytokines, including interleukin (IL) 7 and IL-15, promote immune cell survival and proliferation, and pro-inflammatory cytokines can promote an inflammatory response. Examples of homeostatic cytokines include, but are not limited to, IL-2, IL-4, IL-5, IL-7, IL-10, IL-12p40, IL-12p70, IL-15, and interferon (IFN) gamma. Examples of pro-inflammatory cytokines include, but are not limited to, IL-1a, IL-1b, IL-6, IL-13, IL-17a, tumor necrosis factor (TNF)-alpha, TNF-beta, fibroblast growth factor (FGF) 2, granulocyte macrophage colony-stimulating factor (GM-CSF), soluble intercellular adhesion molecule 1 (sICAM-1), soluble vascular adhesion molecule 1 (sVCAM-1), vascular endothelial growth factor (VEGF), VEGF-C, VEGF-D, and placental growth factor (PLGF). Examples of effectors include, but are not limited to, granzyme A, granzyme B, soluble Fas ligand (sFasL), and perforin. Examples of acute phase-proteins include, but are not limited to, C-reactive protein (CRP) and serum amyloid A (SAA).

“Chemokines” are a type of cytokine that mediates cell chemotaxis, or directional movement. Examples of chemokines include, but are not limited to, IL-8, IL-16, eotaxin, eotaxin-3, macrophage-derived chemokine (MDC or CCL22), monocyte chemotactic protein 1 (MCP-1 or CCL2), MCP-4, macrophage inflammatory protein 1α (MIP-1α, MIP-1α), MIP-1β (MIP-1b), gamma-induced protein 10 (IP-10), and thymus and activation regulated chemokine (TARC or CCL17).

A “therapeutically effective amount,” “effective dose,” “effective amount,” or “therapeutically effective dosage” of a therapeutic agent, e.g., engineered CAR T cells, is any amount that, when used alone or in combination with another therapeutic agent, protects a subject against the onset of a disease or promotes disease regression evidenced by a decrease in severity of disease symptoms, an increase in frequency and duration of disease symptom-free periods, or a prevention of impairment or disability due to the disease affliction. The ability of a therapeutic agent to promote disease regression can be evaluated using a variety of methods known to the skilled practitioner, such as in human subjects during clinical trials, in animal model systems predictive of efficacy in humans, or by assaying the activity of the agent in in vitro assays.

The term “lymphocyte” as used herein includes natural killer (NK) cells, T cells, or B cells. NK cells are a type of cytotoxic (cell toxic) lymphocyte that represent a major component of the inherent immune system. NK cells reject tumors and cells infected by viruses. It works through the process of apoptosis or programmed cell death. They were termed “natural killers” because they do not require activation in order to kill cells. T-cells play a major role in cell-mediated-immunity (no antibody involvement). Its T-cell receptors (TCR) differentiate themselves from other lymphocyte types. The thymus, a specialized organ of the immune system, is primarily responsible for the T cell's maturation. There are six types of T-cells, namely: Helper T-cells (e.g., CD4+ cells), Cytotoxic T-cells (also known as TC, cytotoxic T lymphocyte, CTL, T-killer cell, cytolytic T cell, CD8+ T-cells or killer T cell), Memory T-cells ((i) stem memory T_(SCM) cells, like naive cells, are CD45RO−, CCR7+, CD45RA+, CD62L+(L-selectin), CD27+, CD28+ and IL-7Rα+, but they also express large amounts of CD95, IL-2Rβ, CXCR3, and LFA-1, and show numerous functional attributes distinctive of memory cells); (ii) central memory T_(CM) cells express L-selectin and the CCR7, they secrete IL-2, but not IFNγ or IL-4, and (iii) effector memory TEM cells, however, do not express L-selectin or CCR7 but produce effector cytokines like IFNγ and IL-4), Regulatory T-cells (Tregs, suppressor T cells, or CD4+CD25+ regulatory T cells), Natural Killer T-cells (NKT) and Gamma Delta T-cells. B-cells, on the other hand, play a principal role in humoral immunity (with antibody involvement). It makes antibodies and antigens and performs the role of antigen-presenting cells (APCs) and turns into memory B-cells after activation by antigen interaction. In mammals, immature B-cells are formed in the bone marrow, where its name is derived from.

The term “genetically engineered” or “engineered” refers to a method of modifying the genome of a cell, including, but not limited to, deleting a coding or non-coding region or a portion thereof or inserting a coding region or a portion thereof. In some embodiments, the cell that is modified is a lymphocyte, e.g., a T cell, which can either be obtained from a patient or a donor. The cell can be modified to express an exogenous construct, such as, e.g., a chimeric antigen receptor (CAR) or a T cell receptor (TCR), which is incorporated into the cell's genome.

An “immune response” refers to the action of a cell of the immune system (for example, T lymphocytes, B lymphocytes, natural killer (NK) cells, macrophages, eosinophils, mast cells, dendritic cells and neutrophils) and soluble macromolecules produced by any of these cells or the liver (including Abs, cytokines, and complement) that results in selective targeting, binding to, damage to, destruction of, and/or elimination from a vertebrate's body of invading pathogens, cells or tissues infected with pathogens, cancerous or other abnormal cells, or, in cases of autoimmunity or pathological inflammation, normal human cells or tissues.

The term “immunotherapy” refers to the treatment of a subject afflicted with, or at risk of contracting or suffering a recurrence of, a disease by a method comprising inducing, enhancing, suppressing or otherwise modifying an immune response. Examples of immunotherapy include, but are not limited to, T cell therapies. T cell therapy can include adoptive T cell therapy, tumor-infiltrating lymphocyte (TIL) immunotherapy, autologous cell therapy, engineered autologous cell therapy (eACT), and allogeneic T cell transplantation. However, one of skill in the art would recognize that the conditioning methods disclosed herein would enhance the effectiveness of any transplanted T cell therapy. Examples of T cell therapies are described in U.S. Patent Publication Nos. 2014/0154228 and 2002/0006409, U.S. Pat. No. 5,728,388, and International Publication No. WO 2008/081035.

The T cells of the immunotherapy can come from any source known in the art. For example, T cells can be differentiated in vitro from a hematopoietic stem cell population, or T cells can be obtained from a subject. T cells can be obtained from, e.g., peripheral blood mononuclear cells (PBMCs), bone marrow, lymph node tissue, cord blood, thymus tissue, tissue from a site of infection, ascites, pleural effusion, spleen tissue, and tumors. In addition, the T cells can be derived from one or more T cell lines available in the art. T cells can also be obtained from a unit of blood collected from a subject using any number of techniques known to the skilled artisan, such as FICOLL™ separation and/or apheresis. Additional methods of isolating T cells for a T cell therapy are disclosed in U.S. Patent Publication No. 2013/0287748, which is herein incorporated by references in its entirety.

The term “engineered Autologous Cell Therapy,” which can be abbreviated as “eACT™,” also known as adoptive cell transfer, is a process by which a patient's own T cells are collected and subsequently genetically altered to recognize and target one or more antigens expressed on the cell surface of one or more specific tumor cells or malignancies. T cells can be engineered to express, for example, chimeric antigen receptors (CAR) or T cell receptor (TCR). CAR positive (+) T cells are engineered to express an extracellular single chain variable fragment (scFv) with specificity for a particular tumor antigen linked to an intracellular signaling part comprising at least one costimulatory domain and at least one activating domain. The costimulatory domain can be derived from, e.g., CD28, and the activating domain can be derived from, e.g., CD3-zeta. In certain embodiments, the CAR is designed to have two, three, four, or more costimulatory domains. The CAR scFv can be designed to target, for example, CD19, which is a transmembrane protein expressed by cells in the B cell lineage, including all normal B cells and B cell malignances, including but not limited to NHL, CLL, and non-T cell ALL. In some embodiments, the CAR is engineered such that the costimulatory domain is expressed as a separate polypeptide chain. Example CAR T cell therapies and constructs are described in U.S. Patent Publication Nos. 2013/0287748, 2014/0227237, 2014/0099309, and 2014/0050708, and these references are incorporated by reference in their entirety.

A “patient” as used herein includes any human who is afflicted with a cancer (e.g., a lymphoma or a leukemia). The terms “subject” and “patient” are used interchangeably herein.

As used herein, the term “in vitro cell” refers to any cell which is cultured ex vivo. In particular, an in vitro cell can include a T cell.

The terms “peptide,” “polypeptide,” and “protein” are used interchangeably, and refer to a compound comprised of amino acid residues covalently linked by peptide bonds. A protein or peptide must contain at least two amino acids, and no limitation is placed on the maximum number of amino acids that can comprise a protein's or peptide's sequence. Polypeptides include any peptide or protein comprising two or more amino acids joined to each other by peptide bonds. As used herein, the term refers to both short chains, which also commonly are referred to in the art as peptides, oligopeptides and oligomers, for example, and to longer chains, which generally are referred to in the art as proteins, of which there are many types. “Polypeptides” include, for example, biologically active fragments, substantially homologous polypeptides, oligopeptides, homodimers, heterodimers, variants of polypeptides, modified polypeptides, derivatives, analogs, fusion proteins, among others. The polypeptides include natural peptides, recombinant peptides, synthetic peptides, or a combination thereof.

In some aspects, the polypeptides and/or proteins have deletions from, additions to, and/or substitutions of one or more amino acid of antigen-binding protein, and in some embodiments preferably no more than 8 amino acid substitutions therein. Useful polypeptide fragments may include immunologically functional fragments of antigen binding molecules, including not limited to one or more CDR regions, variable domains of a heavy and/or light chain, a portion of other portions of an antibody chain, and the like. Additionally, polypeptide fragments of activating and/or costimulatory molecules and the like are within the scope of the invention.

“Activation” or “Stimulation” as used herein, refers to a primary response induced by binding of an activating molecule with its cognate ligand, wherein the binding mediates a signal transduction event. An “activating molecule” or “stimulating molecule” refers to a molecule on a T cell, e.g., the TCR/CD3 complex that specifically binds with a cognate stimulatory ligand present on an antigen present cell. Suitable activating molecules are described herein.

A “stimulatory ligand” is a ligand that when present on an antigen presenting cell (e.g., an aAPC, a dendritic cell, a B-cell, and the like) can specifically bind with a stimulatory molecule on a T cell, thereby mediating a primary response by the T cell, including, but not limited to, activation, initiation of an immune response, proliferation, and the like. Stimulatory ligands include, but are not limited to, an MHC Class I molecule loaded with a peptide, an anti-CD3 antibody, a superagonist anti-CD28 antibody, and a superagonist anti-CD2 antibody.

A “costimulatory signal,” as used herein, refers to a signal, which in combination with a primary signal, such as TCR/CD3 ligation, leads to a T cell response, such as, but not limited to, proliferation and/or upregulation or down regulation of key molecules.

A “costimulatory ligand” as used herein, includes a molecule on an antigen presenting cell that specifically binds a cognate co-stimulatory molecule on a T cell. Binding of the costimulatory ligand provides a signal that mediates a T cell response, including, but not limited to, proliferation, activation, differentiation, and the like. A costimulatory ligand induces a signal that is in addition to the primary signal provided by a stimulatory molecule, for instance, by binding of a T cell receptor (TCR)/CD3 complex with a major histocompatibility complex (MHC) molecule loaded with peptide. A co-stimulatory ligand can include, but is not limited to, CD7, B7-1 (CD80), B7-2 (CD86), programmed death (PD) L1, PD-L2, 4-1BB ligand, OX40 ligand, inducible costimulatory ligand (ICOS-L), intercellular adhesion molecule (ICAM), CD30 ligand, CD40, CD70, CD83, human leukocyte antigen G (HLA-G), MHC class I chain-related protein A (MICA), MHC class I chain-related protein B (MICB), herpes virus entry mediator (HVEM), lymphotoxin beta receptor, 3/TR6, immunoglobulin-like transcript (ILT) 3, ILT4, an agonist or antibody that binds Toll ligand receptor and a ligand that specifically binds with B7-H3. A co-stimulatory ligand includes, without limitation, an antibody that specifically binds with a co-stimulatory molecule present on a T cell, such as, but not limited to, CD27, CD28, 4-1BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, tumor necrosis factor superfamily member 14 (TNFSF14 or LIGHT), natural killer cell receptor C (NKG2C), B7-H3, and a ligand that specifically binds with CD83.

A “costimulatory molecule” is a cognate binding partner on a T cell that specifically binds with a costimulatory ligand, thereby mediating a costimulatory response by the T cell, such as, but not limited to, proliferation. Costimulatory molecules include, but are not limited to, CD28, CD28T, OX40, 4-1BB/CD137, CD2, CD3 (alpha, beta, delta, epsilon, gamma, zeta), CD4, CD5, CD7, CD9, CD16, CD22, CD27, CD30, CD 33, CD37, CD40, CD 45, CD64, CD80, CD86, CD134, CD137, CD154, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1 (CD11a/CD18), CD247, CD276 (B7-H3), LIGHT (tumor necrosis factor superfamily member 14; TNFSF14), NKG2C, Ig alpha (CD79a), DAP-10, Fc gamma receptor, MHC class I molecule, TNF, TNFr, integrin, signaling lymphocytic activation molecule, BTLA, Toll ligand receptor, ICAM-1, B7-H3, CDS, ICAM-1, GITR, BAFFR, LIGHT, HVEM (LIGHTR), KIRDS2, SLAMF7, NKp80 (KLRF1), NKp44, NKp30, NKp46, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, ITGAM, CD11b, ITGAX, CD11c, ITGB1, CD29, ITGB2, CD18, LFA-1, ITGB7, NKG2D, TNFR2, TRANCE/RANKL, DNAM1 (CD226), SLAMF4 (CD244, 2B4), CD84, CD96 (Tactile), CEACAM1, CRT AM, Ly9 (CD229), CD160 (BY55), PSGL1, CD100 (SEMA4D), CD69, SLAMF6 (NTB-A, Ly108), SLAM (SLAMF1, CD150, IPO-3), BLAME (SLAMF8), SELPLG (CD162), LTBR, LAT, GADS, SLP-76, PAG/Cbp, CD19a, CD83 ligand, or fragments or combinations thereof.

The terms “reducing” and “decreasing” are used interchangeably herein and indicate any change that is less than the original. “Reducing” and “decreasing” are relative terms, requiring a comparison between pre- and post-measurements. “Reducing” and “decreasing” include complete depletions.

“Treatment” or “treating” of a subject refers to any type of intervention or process performed on, or the administration of an active agent to, the subject with the objective of reversing, alleviating, ameliorating, inhibiting, slowing down or preventing the onset, progression, development, severity or recurrence of a symptom, complication or condition, or biochemical indicia associated with a disease. In one embodiment, “treatment” or “treating” includes a partial remission. In another embodiment, “treatment” or “treating” includes a complete remission.

To calculate percent identity, the sequences being compared are typically aligned in a way that gives the largest match between the sequences. One example of a computer program that can be used to determine percent identity is the GCG program package, which includes GAP (Devereux et al., 1984, Nucl. Acid Res. 12:387; Genetics Computer Group, University of Wisconsin, Madison, Wis.). The computer algorithm GAP is used to align the two polypeptides or polynucleotides for which the percent sequence identity is to be determined. The sequences are aligned for optimal matching of their respective amino acid or nucleotide (the “matched span”, as determined by the algorithm). In certain embodiments, a standard comparison matrix (see, Dayhoff et al., 1978, Atlas of Protein Sequence and Structure 5:345-352 for the PAM 250 comparison matrix; Henikoff et al., 1992, Proc. Natl. Acad. Sci. U.S.A. 89:10915-10919 for the BLOSUM 62 comparison matrix) is also used by the algorithm.

The use of the alternative (e.g., “or”) should be understood to mean either one, both, or any combination thereof of the alternatives. As used herein, the indefinite articles “a” or “an” should be understood to refer to “one or more” of any recited or enumerated component.

The terms “about” or “comprising essentially of” refer to a value or composition that is within an acceptable error range for the particular value or composition as determined by one of ordinary skill in the art, which will depend in part on how the value or composition is measured or determined, i.e., the limitations of the measurement system. For example, “about” or “comprising essentially of” can mean within 1 or more than 1 standard deviation per the practice in the art. Alternatively, “about” or “comprising essentially of” can mean a range of up to 10% (i.e., ±10%). For example, about 3 mg can include any number between 2.7 mg and 3.3 mg (for 10%). Furthermore, particularly with respect to biological systems or processes, the terms can mean up to an order of magnitude or up to 5-fold of a value. When particular values or compositions are provided in the application and claims, unless otherwise stated, the meaning of “about” or “comprising essentially of” should be assumed to be within an acceptable error range for that particular value or composition.

As described herein, any concentration range, percentage range, ratio range or integer range is to be understood to include the value of any integer within the recited range and, when appropriate, fractions thereof (such as one-tenth and one-hundredth of an integer), unless otherwise indicated.

Various aspects of the invention are described in further detail in the following subsections.

II. Binding Molecules and Polynucleotides Encoding the Same

The present invention is directed to a polynucleotide encoding an anti-BCMA antibody or antigen binding molecule thereof which cross competes with one or more antibodies described herein (i.e., one or more described in FIG. 1 ) or an antibody or antigen binding molecule thereof encoded by the polynucleotide. In one embodiment, the invention is directed to a polynucleotide encoding an anti-BCMA antibody or antigen binding molecule thereof which binds to the same epitope as one or more antibodies described in FIG. 1 or an antibody or antigen binding molecule thereof encoded by the polynucleotide. In some embodiments, the polynucleotide encodes an antibody or antigen binding molecule thereof that specifically binds to BCMA, wherein the antibody or binding molecule comprises a heavy chain VH comprising: (a) a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence GX₂X₃X₄X₅X₆X₇SY (SEQ ID NO: 145), wherein: X₂ is not present or G; X₃ is not present or S; X₄ is F, G, I, or Y; X₅ is S or T; X₆ is F or S; and X₇ is S or T; and/or (b) a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃X₄X₅X₆X₇X₈X₉X₁₀YX₁₂X₁₃X₁₄X₁₅X₁₆X₁₇ (SEQ ID NO: 146), wherein: X₁ is A, G, I, S, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is not present or G or S; X₈ is N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₂ is A or N; X₁₃ is D, P, or Q; X₁₄ is K or S; X₁₅ is F, L, or V; X₁₆ is K or Q; and X₁₇ is G or S; and/or (c) a VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇DX₁₉ (SEQ ID NO: 147), wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or A, D, G, P, R, or S; X₅ is not present or E, F, G, L, Q, or T; X₆ is not present or E, M, Q, W, or Y; X₇ is not present or A, E, L, or S; X₈ is not present or G, P, S, or T; X₉ is not present or G, P, or S; X₁₀ is not present or I, L, P, or Y; X₁₁ is not present or W; X₁₂ is not present or H; X₁₃ is not present or E or Y; X₁₄ is not present or D, G, H, P, S, W, or Y; X₁₅ is A, G, L, W, or Y; X₁₆ is not present or A, G, I, P, or V; X₁₇ is F, L, or M; and X₁₉ is I, L, V, or Y.

In one particular embodiment, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VH comprising: (a) a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆SYX₉X₁₀X₁₁ (SEQ ID NO: 263), wherein: X₁ is not present or G; X₂ is not present or S X₃ is F, G, I, or Y; X₄ is S or T; X₅ is F or S; X₆ is S or T; X₉ is A, G, S, or Y; X₁₀ is I, M, or W; and X₁₁ is G, H, N, or S; and/or (b) a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃X₄X₅X₆X₇X₈X₉X₁₀YX₁₂X₁₃X₁₄X₁₅X₁₆X₁₇ (SEQ ID NO: 146), wherein: X₁ is A, G, I, S, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is G or S; X₈ is not present or N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₂ is A or N; X₁₃ is D, P, or Q; X₁₄ is K or S; X₁₅ is F, L, or V; X₁₆ is K or Q; and X₁₇ is G or S; and/or (c) a VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇X₁₈X₁₉DX₂₁ (SEQ ID NO: 264), wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or D, G, or P; X₅ is not present or F, L, or T; X₆ is not present or P, Q, R, W, or Y; X₇ is not present or E, G, L, or S; X₈ is not present or A, G, P, S, or Y; X₉ is not present or A, E, G, P, Q, or S; X₁₀ is not present or E, L, M, PS, T, or Y; X₁₁ is not present or D, G, H, P, S or W; X₁₂ is not present or A, G, I, L, or Y; X₁₃ is not present or A, G, I, V, or W; X₁₄ is not present or H; X₁₅ is not present or Y; X₁₆ is not present or Y; X₁₇ is not present or W or Y; X₁₈ is not present or P or G; X₁₉ is F, L, or M; and X₂₁ is I, L, V, or Y.

In another embodiment, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VL comprising: (a) a VL CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SQX₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅LX₁₇ (SEQ ID NO: 148), wherein X₁ is K or R; X₂ is A or S; X₅ is G or S; X₆ is I, L, or V; X₇ is L or S; X₈ is not present or H or Y; X₉ is not present or S; X₁₀ is not present or N or S; X₁₁ is not present or G or N; X₁₂ is not present or N; X₁₃ is not present or K or Y; X₁₄ is N, R, or S; X₁₅ is N, W, or Y; and X₁₇ is A or D; and/or (b) a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SX₄X₅X₆X₇ (SEQ ID NO: 149), wherein X₁ is D, G, L, S, or W; X₂ is A or G; X₄ is N, S, or T; X₅ is L or R; X₆ is A, E, or Q; and X₇ is S or T; and/or (c) a VL CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁QX₃X₄X₅X₆PX₈T (SEQ ID NO: 150), wherein X₁ is M or Q; X₃ is F, G, H, I, R, or Y; X₄ is A, F, H, I, L, or Y; X₅ is A, G, H, S, T, V, or Y; X₆ is F, L, T, W, or Y; and X₈ is not present or F, L, P, or W.

In one particular embodiment, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VH comprising: (a) a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence GX₂X₃X₄X₅X₆X₇SY (SEQ ID NO: 145), wherein: X₂ is not present or G; X₃ is not present or S; X₄ is F, G, I, or Y; X₅ is S or T; X₆ is F or S; and X₇ is S or T; and/or (b) a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃X₄X₅X₆X₇X₈X₉X₁₀YX₁₂X₁₃X₁₄X₁₅X₁₆X₁₇ (SEQ ID NO: 146), wherein: X₁ is A, G, I, S, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is not present or G or S; X₈ is N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₂ is A or N; X₁₃ is D, P, or Q; X₁₄ is K or S; X₁₅ is F, L, or V; X₁₆ is K or Q; and X₁₇ is G or S; and/or (c) a VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇DX₁₉ (SEQ ID NO: 147), wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or A, D, G, P, R, or S; X₅ is not present or E, F, G, L, Q, or T; X₆ is not present or E, M, Q, W, or Y; X₇ is not present or A, E, L, or S; X₈ is not present or G, P, S, or T; X₉ is not present or G, P, or S; X₁₀ is not present or I, L, P, or Y; X₁₁ is not present or W; X₁₂ is not present or H; X₁₃ is not present or E or Y; X₁₄ is not present or D, G, H, P, S, W, or Y; X₁₅ is A, G, L, W, or Y; X₁₆ is not present or A, G, I, P, or V; X₁₇ is F, L, or M; and X₁₉ is I, L, V, or Y; and/or (d) a VL CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SQX₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅LX₁₇ (SEQ ID NO: 148), wherein X₁ is K or R; X₂ is A or S; X₅ is G or S; X₆ is I, L, or V; X₇ is L or S; X₈ is not present or H or Y; X₉ is not present or S; X₁₀ is not present or N or S; X₁₁ is not present or G or N; X₁₂ is not present or N; X₁₃ is not present or K or Y; X₁₄ is N, R, or S; X₁₅ is N, W, or Y; and X₁₇ is A or D; and/or (e) a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SX₄X₅X₆X₇ (SEQ ID NO: 149), wherein X₁ is D, G, L, S, or W; X₂ is A or G; X₄ is N, S, or T; X₅ is L or R; X₆ is A, E, or Q; and X₇ is S or T; and/or (f) a VL CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁QX₃X₄X₅X₆PX₈T (SEQ ID NO: 150), wherein X₁ is M or Q; X₃ is F, G, H, I, R, or Y; X₄ is A, F, H, I, L, or Y; X₅ is A, G, H, S, T, V, or Y; X₆ is F, L, T, W, or Y; and X₈ is not present or F, L, P, or W.

In one particular embodiment, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VH comprising: (a) a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆SYX₉X₁₀X₁₁ (SEQ ID NO: 263), wherein: X₁ is not present or G; X₂ is not present or S X₃ is F, G, I, or Y; X₄ is S or T; X₅ is F or S; X₆ is S or T; X₉ is A, G, S, or Y; X₁₀ is I, M, or W; and X₁₁ is G, H, N, or S; and/or (b) a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃X₄X₅X₆X₇X₈X₉X₁₀YX₁₂X₁₃X₁₄X₁₅X₁₆X₁₇ (SEQ ID NO: 146), wherein: X₁ is A, G, I, S, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is G or S; X₈ is not present or N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₂ is A or N; X₁₃ is D, P, or Q; X₁₄ is K or S; X₁₅ is F, L, or V; X₁₆ is K or Q; and X₁₇ is G or S; and/or (c) a VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇X₁₈X₁₉DX₂₁ (SEQ ID NO: 264), wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or D, G, or P; X₅ is not present or F, L, or T; X₆ is not present or P, Q, R, W, or Y; X₇ is not present or E, G, L, or S; X₈ is not present or A, G, P, S, or Y; X₉ is not present or A, E, G, P, Q, or S; X₁₀ is not present or E, L, M, PS, T, or Y; X₁₁ is not present or D, G, H, P, S or W; X₁₂ is not present or A, G, I, L, or Y; X₁₃ is not present or A, G, I, V, or W; X₁₄ is not present or H; X₁₅ is not present or Y; X₁₆ is not present or Y; X₁₇ is not present or W or Y; X₁₈ is not present or P or G; X₁₉ is F, L, or M; and X₂₁ is I, L, V, or Y; and/or (d) a VL CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SQX₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅LX₁₇ (SEQ ID NO: 148), wherein X₁ is K or R; X₂ is A or S; X₅ is G or S; X₆ is I, L, or V; X₇ is L or S; X₈ is not present or H or Y; X₉ is not present or S; X₁₀ is not present or N or S; X₁₁ is not present or G or N; X₁₂ is not present or N; X₁₃ is not present or K or Y; X₁₄ is N, R, or S; X₁₅ is N, W, or Y; and X₁₇ is A or D; and/or (e) a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SX₄X₅X₆X₇ (SEQ ID NO: 149), wherein X₁ is D, G, L, S, or W; X₂ is A or G; X₄ is N, S, or T; X₅ is L or R; X₆ is A, E, or Q; and X₇ is S or T; and/or (f) a VL CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁QX₃X₄X₅X₆PX₈T (SEQ ID NO: 150), wherein X₁ is M or Q; X₃ is F, G, H, I, R, or Y; X₄ is A, F, H, I, L, or Y; X₅ is A, G, H, S, T, V, or Y; X₆ is F, L, T, W, or Y; and X₈ is not present or F, L, P, or W.

In another embodiment, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VH and a VL, wherein: (i) the VH comprises: (a) a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence GX₂X₃X₄X₅X₆X₇SY (SEQ ID NO: 145), wherein: X₂ is not present or G; X₃ is not present or S; X₄ is F, G, I, or Y; X₅ is S or T; X₆ is F or S; and X₇ is S or T; and/or (b) a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃X₄X₅X₆X₇X₈X₉X₁₀YX₁₂X₁₃X₁₄X₁₅X₁₆X₁₇ (SEQ ID NO: 146), wherein: X₁ is A, G, I, S, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is not present or G or S; X₈ is N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₂ is A or N; X₁₃ is D, P, or Q; X₁₄ is K or S; X₁₅ is F, L, or V; X₁₆ is K or Q; and X₁₇ is G or S; and/or (c) a VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇DX₁₉ (SEQ ID NO: 147), wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or A, D, G, P, R, or S; X₅ is not present or E, F, G, L, Q, or T; X₆ is not present or E, M, Q, W, or Y; X₇ is not present or A, E, L, or S; X₈ is not present or G, P, S, or T; X₉ is not present or G, P, or S; X₁₀ is not present or I, L, P, or Y; X₁₁ is not present or W; X₁₂ is not present or H; X₁₃ is not present or E or Y; X₁₄ is not present or D, G, H, P, S, W, or Y; X₁₅ is A, G, L, W, or Y; X₁₆ is not present or A, G, I, P, or V; X₁₇ is F, L, or M; and X₁₉ is I, L, V, or Y; and (ii) the VL comprises: (a) a VL CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SQX₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅LX₁₇ (SEQ ID NO: 148), wherein X₁ is K or R; X₂ is A or S; X₅ is G or S; X₆ is I, L, or V; X₇ is L or S; X₈ is not present or H or Y; X₉ is not present or S; X₁₀ is not present or N or S; X₁₁ is not present or G or N; X₁₂ is not present or N; X₁₃ is not present or K or Y; X₁₄ is N, R, or S; X₁₅ is N, W, or Y; and X₁₇ is A or D; and/or (b) a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SX₄X₅X₆X₇ (SEQ ID NO: 149), wherein X₁ is D, G, L, S, or W; X₂ is A or G; X₄ is N, S, or T; X₅ is L or R; X₆ is A, E, or Q; and X₇ is S or T; and/or (c) a VL CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁QX₃X₄X₅X₆PX₈T (SEQ ID NO: 150), wherein X₁ is M or Q; X₃ is F, G, H, I, R, or Y; X₄ is A, F, H, I, L, or Y; X₅ is A, G, H, S, T, V, or Y; X₆ is F, L, T, W, or Y; and X₈ is not present or F, L, P, or W.

In another embodiment, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VH and a VL, wherein: (i) the VH comprises: (a) a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆SYX₉X₁₀X₁₁ (SEQ ID NO: 263), wherein: X₁ is not present or G; X₂ is not present or S X₃ is F, G, I, or Y; X₄ is S or T; X₅ is F or S; X₆ is S or T; X₉ is A, G, S, or Y; X₁₀ is I, M, or W; and X₁₁ is G, H, N, or S; and/or (b) a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃X₄X₅X₆X₇X₈X₉X₁₀YX₁₂X₁₃X₁₄X₁₅X₁₆X₁₇ (SEQ ID NO: 146), wherein: X₁ is A, G, I, S, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is G or S; X₈ is not present or N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₂ is A or N; X₁₃ is D, P, or Q; X₁₄ is K or S; X₁₅ is F, L, or V; X₁₆ is K or Q; and X₁₇ is G or S; and/or (c) a VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇X₁₈X₁₉DX₂₁ (SEQ ID NO: 264), wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or D, G, or P; X₅ is not present or F, L, or T; X₆ is not present or P, Q, R, W, or Y; X₇ is not present or E, G, L, or S; X₈ is not present or A, G, P, S, or Y; X₉ is not present or A, E, G, P, Q, or S; X₁₀ is not present or E, L, M, P, S, T, or Y; X₁₁ is not present or D, G, H, P, S or W; X₁₂ is not present or A, G, I, L, or Y; X₁₃ is not present or A, G, I, V, or W; X₁₄ is not present or H; X₁₅ is not present or Y; X₁₆ is not present or Y; X₁₇ is not present or W or Y; X₁₈ is not present or P or G; X₁₉ is F, L, or M; and X₂₁ is I, L, V, or Y; and (ii) the VL comprises: (a) a VL CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SQX₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅LX₁₇ (SEQ ID NO: 148), wherein X₁ is K or R; X₂ is A or S; X₅ is G or S; X₆ is I, L, or V; X₇ is L or S; X₈ is not present or H or Y; X₉ is not present or S; X₁₀ is not present or N or S; X₁₁ is not present or G or N; X₁₂ is not present or N; X₁₃ is not present or K or Y; X₁₄ is N, R, or S; X₁₅ is N, W, or Y; and X₁₇ is A or D; and/or (b) a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SX₄X₅X₆X₇ (SEQ ID NO: 149), wherein X₁ is D, G, L, S, or W; X₂ is A or G; X₄ is N, S, or T; X₅ is L or R; X₆ is A, E, or Q; and X₇ is S or T; and/or (c) a VL CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁QX₃X₄X₅X₆PX₈T (SEQ ID NO: 150), wherein X₁ is M or Q; X₃ is F, G, H, I, R, or Y; X₄ is A, F, H, I, L, or Y; X₅ is A, G, H, S, T, V, or Y; X₆ is F, L, T, W, or Y; and X₈ is not present or F, L, P, or W.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence GX₂X₃X₄X₅X₆X₇SY (SEQ ID NO: 145), wherein: X₂ is not present or G; X₃ is not present or S; X₄ is F, G, I, or Y; X₅ is S or T; X₆ is F or S; and X₇ is S or T.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence GX₂TFSSY (SEQ ID NO: 151), wherein: X₂ is F or G.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence GX₂X₃X₄X₅X₆SSY (SEQ ID NO: 152), wherein: X₂ is not present or G; X₃ is not present or S; X₄ is F, G, or I; X₅ is S or T; and X₆ is F or S.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆SYX₉X₁₀X₁₁ (SEQ ID NO: 263), wherein: X₁ is not present or G; X₂ is not present or S X₃ is F, G, I, or Y; X₄ is S or T; X₅ is F or S; X₆ is S or T; X₉ is A, G, S, or Y; X₁₀ is I, M, or W; and X₁₁ is G, H, N, or S.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁TFX₄SYX₇X₈X₉ (SEQ ID NO: 265), wherein: X₁ is F, G, or Y; X₄ is S or T; X₇ is A, G, S, or Y; X₈ is I or M; and X₉ is H, N, or S.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence FTFSSYX₇MX₉ (SEQ ID NO: 266), wherein: X₇ is A, G, or S; and X₉ is H, N, or S.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃X₄X₅X₆X₇X₈X₉X₁₀YX₁₂X₁₃X₁₄X₁₅X₁₆X₁₇ (SEQ ID NO: 146), wherein: X₁ is A, G, I, S, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is G or S; X₈ is not present or N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₂ is A or N; X₁₃ is D, P, or Q; X₁₄ is K or S; X₁₅ is F, L, or V; X₁₆ is K or Q; and X₁₇ is G or S.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃X₄X₅X₆X₇X₈X₉X₁₀YAX₁₃X₁₄X₁₅X₁₆G (SEQ ID NO: 153), wherein: X₁ is A, G, I, T, or V; X₃ is I, N, or S; X₄ is G, P, S, or Y; X₅ is D, G, I, or S; X₆ is F, G, or S; X₇ is G or S; X₈ is N, S, or T; X₉ is A, I, K, or T; X₁₀ is N, S, or Y; X₁₃ is D or Q; X₁₄ is K or S; X₁₅ is F or V; and X₁₆ is K or Q.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁ISX₄X₅X₆X₇X₈X₉YYADSVKG (SEQ ID NO: 154), wherein: X₁ is A, T, or V; X₄ is G, S, or Y; X₅ is D or S; X₆ is G or S; X₇ is G or S; X₈ is N, S, or T; and X₉ is I, K, or T.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VH CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁IX₃PX₅X₆GX₈X₉X₁₀YAQKFQG (SEQ ID NO: 155), wherein: X₁ is G or I; X₃ is I or N; X₅ is G or I; X₆ is F or G; X₈ is S or T; X₉ is A or T; and X₁₀ is N or S.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises three VH CDRs and three VL CDRs, wherein the VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇DX₁₉ (SEQ ID NO: 147) and wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or A, D, G, P, R, or S; X₅ is not present or E, F, G, L, Q, or T; X₆ is not present or E, M, Q, W, or Y; X₇ is not present or A, E, L, or S; X₈ is not present or G, P, S, or T; X₉ is not present or G, P, or S; X₁₀ is not present or I, L, P, or Y; X₁₁ is not present or W; X₁₂ is not present or H; X₁₃ is not present or E or Y; X₁₄ is not present or D, G, H, P, S, W, or Y; X₁₅ is A, G, L, W, or Y; X₁₆ is not present or A, G, I, P, or V; X₁₇ is F, L, or M; and X₁₉ is I, L, V, or Y.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises three VH CDRs and three VL CDRs, wherein the VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence ARX₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇DX₁₉ (SEQ ID NO: 156) and wherein: X₃ is not present or D, G, or T; X₄ is not present or A, D, G, P, R, or S; X₅ is not present or E, F, G, Q, or T; X₆ is not present or E, M, W, or Y; X₇ is not present or A, L, or S; X₈ is not present or G, S, or T; X₉ is not present or G or S; X₁₀ is not present or I, L, or P; X₁₁ is not present or W; X₁₂ is not present or H; X₁₃ is not present or E or Y; X₁₄ is not present or G, H, P, S, W, or Y; X₁₅ is A, G, L, W, or Y; X₁₆ is not present or A, G, I, P, or V; X₁₇ is F, L, or M; and X₁₉ is I, L, V, or Y.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises three VH CDRs and three VL CDRs, wherein the VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂X₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇X₁₈X₁₉DX₂₁ (SEQ ID NO: 264) and wherein: X₁ is A or V; X₂ is K or R; X₃ is not present or D, G, or T; X₄ is not present or D, G, or P; X₅ is not present or F, L, or T; X₆ is not present or P, Q, R, W, or Y; X₇ is not present or E, G, L, or S; X₈ is not present or A, G, P, S, or Y; X₉ is A, E, G, P, Q, or S; X₁₀ is E, L, M, P, S, T, or Y; X₁₁ is not present or D, G, H, P, S or W; X₁₂ is not present or A, G, I, L, or Y; X₁₃ is not present or A, G, I, V, or W; X₁₄ is not present or H; X₁₅ is not present or Y; X₁₆ is not present or Y; X₁₇ is not present or W or Y; X₁₈ is not present or P or G; X₁₉ is F, L, or M; and X₂₁ is I, L, V, or Y.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises three VH CDRs and three VL CDRs, wherein the VH CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence ARX₃X₄X₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅X₁₆X₁₇X₁₈X₁₉DX₂₁ (SEQ ID NO: 267), wherein: X₃ is not present or D or T; X₄ is not present or D or G; X₅ is not present or F or T; X₆ is not present or P, R, W, or Y; X₇ is not present or E, G, L, or S; X₈ is not present or A, G, S, or Y; X₉ is A, E, G, Q, or S; X₁₀ is E, L, M, P, S, or T; X₁₁ is not present or G, H, P, S or W; X₁₂ is not present or A, G, I, L, or Y; X₁₃ is not present or A, I, V, or W; X₁₄ is not present or H; X₁₅ is not present or Y; X₁₆ is not present or Y; X₁₇ is not present or W or Y; X₁₈ is not present or P or G; X₁₉ is F, L, or M; and X₂₁ is I, L, V, or Y.

In some embodiments, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises one, two, or all three of any of the VH CDRs listed above or described in FIG. 1A or FIG. 1B. In some embodiments, the antibody or antigen binding molecule comprises the VH framework regions (FRs) described herein. In specific embodiments, the antibody or antigen binding molecule comprises the VH FRs of an antibody set forth in FIG. 1A or FIG. 1B (e.g., one, two, three, or four of the FRs in one sequence of FIG. 1A).

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VL CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SQX₅X₆X₇X₈X₉X₁₀X₁₁X₁₂X₁₃X₁₄X₁₅LX₁₇ (SEQ ID NO: 148), wherein: X₁ is K or R; X₂ is A or S; X₅ is G or S; X₆ is I, L, or V; X₇ is L or S; X₈ is not present or H or Y; X₉ is not present or S; X₁₀ is not present or N or S; X₁₁ is not present or G or N; X₁₂ is not present or N; X₁₃ is not present or K or Y; X₁₄ is N, R, or S; X₁₅ is N, W, or Y; and X₁₇ is A or D.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VL CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence RASQX₅X₆SX₈X₉LA (SEQ ID NO: 157), wherein: X₅ is G or S; X₆ is I or V; X₈ is R or S; and X₉ is N, W, or Y.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VL CDR1 comprising, consisting of, or consisting essentially of the amino acid sequence X₁SSQSX₆LX₈SX₁₀X₁₁X₁₂X₁₃NYLX₁₇ (SEQ ID NO: 158), wherein: X₁ is K or R; X₆ is L or V; X₈ is H or Y; X₁₀ is N or S; X₁₁ is G or N; X₁₂ is not present or N; X₁₃ is K or Y; and X₁₇ is A or D.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SX₄X₅X₆X₇ (SEQ ID NO: 149), wherein: X₁ is D, G, L, S, or W; X₂ is A or G; X₄ is N, S, or T; X₅ is L or R; X₆ is A, E, or Q; and X₇ is S or T.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁ASX₄RAT (SEQ ID NO: 159), wherein: X₁ is D, G, or S; and X₄ is N or T.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁ASX₄X₅X₆X₇ (SEQ ID NO: 160), wherein: X₁ is D, G, or S; X₄ is N, S, or T; X₅ is L or R; X₆ is A or Q; and X₇ is S or T.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VL CDR2 comprising, consisting of, or consisting essentially of the amino acid sequence X₁X₂SX₄RX₆S (SEQ ID NO: 161), wherein X₁ is L or W; X₂ is A or G; X₄ is N or T; and X₆ is A or E.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VL CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence X₁QX₃X₄X₅X₆PX₈T (SEQ ID NO: 150), wherein: X₁ is M or Q; X₃ is F, G, H, I, R, or Y; X₄ is A, F, H, I, L, or Y; X₅ is A, G, H, S, T, V, or Y; X₆ is F, L, T, W, or Y; and X₈ is not present or F, L, P, or W.

In one embodiment, the antibody or antigen binding molecule, which specifically binds to BCMA (e.g., hBCMA), comprises a VL CDR3 comprising, consisting of, or consisting essentially of the amino acid sequence QQX₃X₄X₅X₆PX₈T (SEQ ID NO: 162), wherein: X₃ is H, I, R, or Y; X₄ is A, F, H, I, or Y; X₅ is A, S, T, V, or Y; X₆ is F, W, or Y; and X₈ is not present or F, L, P, or W.

In some embodiments, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises one, two, or all three of any of the VL CDRs listed above or described in FIG. 2 . In some embodiments, the antibody or antigen binding molecule comprises the VL framework regions (FRs) described herein. In specific embodiments, the antibody or antigen binding molecule comprises the VL FRs of an antibody set forth in FIG. 4 (e.g., one, two, three, or four of the FRs in one row of FIG. 4 ).

In some embodiments, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VH CDR1, wherein the VH CDR1 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 9-16. In other embodiments, the antibody or antigen binding molecule comprises a VH CDR1, wherein the VH CDR1 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 215-222. In some embodiments, the antibody or antigen binding molecule comprises a VH CDR2, wherein the VH CDR2 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 25-32. In some embodiments, the antibody or antigen binding molecule comprises a VH CDR2, wherein the VH CDR2 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 231-238. In some embodiments, the antibody or antigen binding molecule comprises a VH CDR3, wherein the VH CDR3 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 41-48. In some embodiments, the antibody or antigen binding molecule comprises a VH CDR3, wherein the VH CDR3 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 247-254.

In some embodiments, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VH CDR1, a VH CDR2, and VH CDR3, wherein the VH CDR1, VH CDR2, and VH CDR3 comprise the amino acid sequence of the VH CDR1, VH CDR2, and VH CDR3 of an antibody in FIG. 1A or FIG. 1B, respectively.

In some embodiments, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VL CDR1, wherein the VL CDR1 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 81-88. In some embodiments, the antibody or antigen binding molecule comprises a VL CDR2, wherein the VL CDR2 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 97-104. In some embodiments, the antibody or antigen binding molecule comprises a VL CDR3, wherein the VL CDR3 comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 113-120.

In some embodiments, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VL CDR1, a VL CDR2, and VL CDR3, wherein the VL CDR1, VL CDR2, and VL CDR3 comprise the amino acid sequence of the VL CDR1, VL CDR2, and VL CDR3 of an antibody in FIG. 1C, respectively.

In some embodiments, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises a VH framework region 1 (FR1), wherein the VH FR1 comprises an amino acid sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from SEQ ID NOs: 1-8 and 207-214. In some embodiments, the antibody or antigen binding molecule comprises a VH FR2, wherein the VH FR2 comprises an amino acid sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from SEQ ID NOs: 17-24 and 223-23. In some embodiments, the antibody or antigen binding molecule comprises a VH FR3, wherein the VH FR3 comprises an amino acid sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from SEQ ID NOs: 33-40 and 239-246. In some embodiments, the antibody or antigen binding molecule comprises a VH FR4, wherein the VH FR4 comprises an amino acid sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from SEQ ID NOs: 49-56 and 255-262.

In some embodiments, the antibody or antigen binding molecule or a fragment thereof comprises a VL FR1, wherein the VL FR1 comprises an amino acid sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from SEQ ID NOs: 73-80. In some embodiments, the antibody or antigen binding molecule or a fragment thereof comprises a VL FR2, wherein the VL FR2 comprises an amino acid sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from SEQ ID NOs: 89-96. In some embodiments, the antibody or antigen binding molecule or a fragment thereof comprises a VL FR3, wherein the VL FR3 comprises an amino acid sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from SEQ ID NOs: 105-112. In some embodiments, the antibody or antigen binding molecule or a fragment thereof comprises a VL FR4, wherein the VL FR4 comprises an amino acid sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from SEQ ID NOs: 121-128.

In some embodiments, the polynucleotide encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule comprises any one, two, and/or three VH CDR sequences disclosed herein. In certain embodiments, the antibody or antigen binding molecule comprises a VH CDR1, a VH CDR2, and a VH CDR3 having the amino acid sequence of any VH CDR1, VH CDR2, and VH CDR3 disclosed herein, respectively. In some embodiments, the antibody or antigen binding molecule comprises any one, two, and/or three VL CDR sequences disclosed herein. In certain embodiments, the antibody or antigen binding molecule comprises a VL CDR1, a VL CDR2, and a VL CDR3 having the amino acid sequence of any VL CDR1, VL CDR2, and VL CDR3 disclosed herein, respectively.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 9; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 25; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 41; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 81; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 97; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 113.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 10; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 26; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 42; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 82; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 98; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 114.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 11; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 27; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 43; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 83; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 99; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 115.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 12; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 28; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 44; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 84; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 100; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 116.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 13; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 29; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 45; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 85; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 101; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 117.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 14; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 30; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 46; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 86; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 102; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 118.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 15; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 31; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 47; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 87; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 103; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 119.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 16; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 32; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 48; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 88; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 104; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 120.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 215; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 231; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 247; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 81; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 97; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 113.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 216; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 232; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 248; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 82; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 98; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 114.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 217; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 233; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 249; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 83; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 99; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 115.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO:218; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 234; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 250; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 84; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 100; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 116.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 219; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 235; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 251; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 85; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 101; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 117.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 220; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 236; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 252; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 86; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 102; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 118.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 221; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 237; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 253; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 87; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 103; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 119.

In one embodiment, the antibody or antigen binding molecule comprises: (a) a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 222; (b) a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 238; (c) a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 254; (d) a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 88; (e) a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 104; and (f) a VL CDR3 region comprising the amino acid sequence of SEQ ID NO: 120.

In some embodiments, the antibody or antigen binding molecule comprises a heavy chain variable region sequence comprising an amino acid sequence of FIG. 1A or FIG. 1B. In some embodiments, the antibody or antigen binding molecule comprises a heavy chain variable region sequence comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 65-72. In some embodiments, the antibody or antigen binding molecule comprises a light chain variable region sequence comprising an amino acid sequence selected from FIG. 1C. In some embodiments, the antibody or antigen binding molecule comprises a light chain variable region sequence comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 137-144.

In some embodiments, the antibody or antigen binding molecule comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 65; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO 137.

In some embodiments, the antibody or antigen binding molecule comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 66; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 138.

In some embodiments, the antibody or antigen binding molecule comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 67; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 139.

In some embodiments, the antibody or antigen binding molecule comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 68; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 140.

In some embodiments, the antibody or antigen binding molecule comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 69; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 141.

In some embodiments, the antibody or antigen binding molecule comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 70; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 142.

In some embodiments, the antibody or antigen binding molecule comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 71; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 143.

In some embodiments, the antibody or antigen binding molecule comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 72; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 144.

In one particular embodiment, the polynucleotide of the present invention comprises a nucleotide sequence at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or about 100% identical to a nucleotide sequence selected form the group consisting of SEQ ID NOs: 57-64. In another embodiment, the polynucleotide of the present invention comprises a nucleotide sequence at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or about 100% identical to a nucleotide sequence selected form the group consisting of SEQ ID NOs: 129-136.

The antibody or antigen binding molecule encoded by the polypeptide of the present invention can be single chained or double chained. In some embodiments, the antibody or antigen binding molecule comprises is single chained. In certain embodiments, the antigen binding molecule is selected from the group consisting of an scFv, an Fab, an Fab′, an Fv, an F(ab′)2, a dAb, and any combination thereof. In one particular embodiment, the antibody or antigen binding molecule comprises an scFv.

In certain embodiments, the antibody or antigen binding molecule comprises a single chain, wherein the heavy chain variable region and the light chain variable region are connected by a linker. In some embodiments, the VH is located at the N terminus of the linker and the VL is located at the C terminus of the linker. In other embodiments, the VL is located at the N terminus of the linker and the VH is located at the C terminus of the linker. In some embodiments, the linker comprises at least about 5, at least about 8, at least about 10, at least about 13, at least about 15, at least about 18, at least about 20, at least about 25, at least about 30, at least about 35, at least about 40, at least about 45, at least about 50, at least about 60, at least about 70, at least about 80, at least about 90, or at least about 100 amino acids. In some embodiments, the linker comprises at least about 18 amino acids. In certain embodiments, the linker comprises an amino acid sequence that is at least about 75%, at least about 85%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to the amino acid sequence GSTSGSGKPGSGEGSTKG (SEQ ID NO: 174) or a poly-Gly linker such as the amino acid sequence GGGGSGGGGSGGGGS (SEQ ID NO: 268). Or GGGGSGGGGSGGGGSGGGGS (SEQ ID NO: 411). In one embodiment, the linker is a Whitlow linker. In certain embodiments, the antibody or antigen binding molecule comprises a single chain, wherein the heavy chain variable region and the light chain variable region are connected by a linker, wherein the linker comprises the amino acid sequence of SEQ ID NO: 174.

In some embodiments, the antibody or antigen binding molecules of the present invention specifically bind BCMA (e.g., hBCMA). In certain embodiments, an anti-BCMA antibody or antigen binding molecule of the present invention binds human BCMA with a K_(D) of less than 1×10⁻⁶ M, less than 1×10⁻⁷ M, less than 1×10⁻⁸M, or less than 1×10⁻⁹ M. In one particular embodiment, the anti-BCMA antibody or antigen binding molecules binds human BCMA with a K_(D) of less than 1×10⁻⁷ M. In another embodiment, the anti-BCMA antibody or antigen binding molecules binds human BCMA with a K_(D) of less than 1×10⁻⁸ M. In some embodiments, the anti-BCMA antibody or antigen binding molecules binds human BCMA with a K_(D) of about 1×10⁻⁷ M, about 2×10⁻⁷ M, about 3×10⁻⁷ M, about 4×10⁻⁷ M, about 5×10⁻⁷ M, about 6×10⁻⁷ M, about 7×10⁻⁷ M, about 8×10⁻⁷ M, about 9×10⁻⁷ M, about 1×10⁻⁸ M, about 2×10⁻⁸ M, about 3×10⁻⁸M, about 4×10⁻⁸M, about 5×10⁻⁸ M, about 6×10⁻⁸ M, about 7×10⁻⁸ M, about 8×10⁻⁸ M, about 9×10⁻⁸ M, about 1×10⁻⁹M, about 2×10⁻⁹M, about 3×10⁻⁹ M, about 4×10⁻⁹M, about 5×10⁻⁹ M, about 6×10⁻⁹ M, about 7×10⁻⁹ M, about 8×10⁻⁹M, about 9×10⁻⁹M, about 1×10⁻¹⁰ M, or about 5×10⁻¹⁰ M. In certain embodiments, the K_(D) is calculated as the quotient of k_(off)/k_(on), and the k_(on) and k_(off) are determined using a monovalent antibody, such as a Fab fragment, as measured by, e.g., BIAcore® surface plasmon resonance technology. In other embodiments, the K_(D) is calculated as the quotient of k_(off)/k_(on), and the k_(on) and k_(off) are determined using a bivalent antibody, such as a Fab fragment, as measured by, e.g., BIAcore® surface plasmon resonance technology.

In other embodiments, the anti-BCMA antibody or antigen binding molecule binds human BCMA-Fc with a K_(D) of less than 1×10⁻⁹M, less than 3×10⁻⁹M, less than 5×10⁻⁹M, less than 1×10⁻¹⁰M, less than 3×10⁻¹⁰M, or less than 5×10⁻¹⁰M. In other embodiments, the anti-BCMA antibody or antigen binding molecules binds cyno BCMA-Fc with a K_(D) of less than 1×10⁻⁵M, less than 1×10⁻⁶ M, less than 1×10⁻⁷M, less than 1×10⁻⁸ M, less than 1×10⁻⁹M, or less than 1×10⁻¹⁰ M.

In some embodiments, the anti-BCMA antibody or antigen binding molecule binds human BCMA with an association rate (k_(on)) of less than 1×10⁻⁴M⁻¹ s⁻¹, less than 2×10⁻⁴M⁻¹ s⁻¹, less than 3×10⁻⁴ M⁻¹ s⁻¹, less than 4×10⁻⁴M⁻¹ s⁻¹, less than 5×10⁻⁴M⁻¹ s⁻¹, less than 6×10⁻⁴ M⁻¹ s⁻¹, less than 7×10⁻⁴ M⁻¹ s⁻¹, less than 8×10⁻⁴M⁻¹ s⁻¹, less than 9×10⁻⁴ M⁻¹ s⁻¹, less than 1×10⁻⁵M⁻¹ s⁻¹, less than 2×10⁻⁵ M⁻¹ s⁻¹, less than 3×10⁻⁵M⁻¹ s⁻¹, less than 4×10⁻⁵ M⁻¹ s⁻¹, less than 5×10⁻⁵ M⁻¹ s⁻¹, less than 6×10⁻⁵M⁻¹ s⁻¹, less than 7×10⁻⁵M⁻¹ s⁻¹, less than 8×10⁻⁵ M⁻¹ s⁻¹, less than 9×10⁻⁵ M⁻¹ s⁻¹, less than 1×10⁻⁶M⁻¹ s⁻¹, less than 2×10⁻⁶ M⁻¹ s⁻¹, less than 3×10⁻⁶M⁻¹ s⁻¹, less than 4×10⁻⁶ M⁻¹ s⁻¹, less than 5×10⁻⁶M⁻¹ s⁻¹, less than 6×10⁻⁶ M⁻¹ s⁻¹, less than 7×10⁻⁶ M⁻¹ s⁻¹, less than 8×10⁻⁶M⁻¹ s⁻¹, less than 9×10⁻⁶M⁻¹ s⁻¹, or less than 1×10⁻⁷M⁻¹s⁻¹. In certain embodiments, the k_(on) is determined using a monovalent antibody, such as a Fab fragment, as measured by, e.g., BIAcore® surface plasmon resonance technology. In other embodiments, the k_(on) is determined using a bivalent antibody as measured by, e.g., BIAcore® surface plasmon resonance technology.

In some embodiments, the anti-BCMA antibody or antigen binding molecule binds human BCMA with an dissociation rate (k_(off)) of less than 1×10⁻² s⁻¹, less than 2×10⁻² s⁻¹, less than 3×10⁻² s⁻¹, less than 4×10⁻² s⁻¹, less than 5×10⁻² s⁻¹, less than 6×10⁻² s⁻¹, less than 7×10⁻² s⁻¹, less than 8×10⁻² s⁻¹, less than 9×10⁻² s⁻¹, less than 1×10⁻³ s⁻¹, less than 2×10⁻³ s⁻¹, less than 3×10⁻³ s⁻¹, less than 4×10⁻³ s⁻¹, less than 5×10⁻³ s⁻¹, less than 6×10⁻³ s⁻¹, less than 7×10⁻³ s⁻¹, less than 8×10⁻³ s⁻¹, less than 9×10⁻³ s⁻¹, less than 1×10⁻⁴ s⁻¹, less than 2×10⁻⁴ s⁻¹, less than 3×10⁻⁴ s⁻¹, less than 4×10⁻⁴ s⁻¹, less than 5×10⁻⁴s⁻¹, less than 6×10⁻⁴ s⁻¹, less than 7×10⁻⁴ s⁻¹, less than 8×10⁻⁴ s⁻¹, less than 9×10⁻⁴ s⁻¹, less than 1×10⁻⁴ s⁻¹, or less than 5×10⁻⁴ s⁻¹. In certain embodiments, the k_(off) is determined using a monovalent antibody, such as a Fab fragment, as measured by, e.g., BIAcore® surface plasmon resonance technology. In other embodiments, the k_(off) is determined using a bivalent antibody as measured by, e.g., BIAcore® surface plasmon resonance technology.

In some embodiments, the polynucleotide of the present invention encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule cross competes with a reference antibody disclosed herein. In certain embodiments, the antibody or antigen binding molecule cross competes with a reference antibody comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-56, 65-128, and 137-144. In some embodiments, the antibody or antigen binding molecule cross competes with a reference antibody comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 65-72 and 137-144. In certain embodiments, the antibody or antigen binding molecule cross competes with a reference antibody, wherein the reference antibody comprises a VH CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 9-16. In certain embodiments, the antibody or antigen binding molecule cross competes with a reference antibody, wherein the reference antibody comprises a VH CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 25-32. In certain embodiments, the antibody or antigen binding molecule cross competes with a reference antibody, wherein the reference antibody comprises a VH CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 41-48. In some embodiments, the antibody or antigen binding molecule cross competes with a reference antibody, wherein the reference antibody comprises a VL CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 89-96. In certain embodiments, the antibody or antigen binding molecule cross competes with a reference antibody, wherein the reference antibody comprises a VL CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 105-112. In certain embodiments, the antibody or antigen binding molecule cross competes with a reference antibody, wherein the reference antibody comprises a VL CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 121-128. In one embodiment, the antibody or antigen binding molecule cross competes with a reference antibody, wherein the reference antibody comprises a VH comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 65-72. In another embodiment, the antibody or antigen binding molecule cross competes with a reference antibody, wherein the reference antibody comprises a VL comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 137-144.

In some embodiments, the polynucleotide of the present invention encodes an antibody or antigen binding molecule that specifically binds to BCMA, wherein the antibody or antigen binding molecule binds the same or an overlapping epitope as a reference antibody disclosed herein (e.g., FIG. 1 ). In certain embodiments, the antibody or antigen binding molecule binds the same or an overlapping epitope as a reference antibody comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-56, 65-128, and 137-144. In some embodiments, the antibody or antigen binding molecule binds the same or an overlapping epitope as a reference antibody comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 65-72 and 137-144.

III. Polynucleotides Encoding Chimeric Antigen Receptors and T Cell Receptors

The present invention is also directed to polynucleotides encoding chimeric antigen receptors (CARs) or T cell receptors (TCRs) comprising an antigen binding molecule that specifically binds to BCMA described in Section II, and engineered T cells comprising an antigen binding molecule that specifically binds to BCMA described in Section II. In some embodiments, an anti-BCMA CAR or TCR encoded by the polynucleotide of the present invention comprises an antigen binding molecule that specifically binds to BCMA. In some embodiments, the anti-BCMA CAR or TCR encoded by the polynucleotide further comprises a costimulatory domain. In some embodiments, the costimulatory domain in the anti-BCMA CAR or TCR encoded by the polynucleotide comprises an extracellular domain (i.e., a hinge region), a transmembrane domain, and/or an intracellular (signaling) domain. In some embodiments, the anti-BCMA CAR or TCR encoded by the polynucleotide further comprises a CD3 zeta activating domain. In one particular embodiment, the anti-BCMA CAR or TCR encoded by the polynucleotide comprises an antigen binding molecule that specifically binds BCMA (e.g., hBCMA), a costimulatory domain comprising an extracellular domain, a transmembrane domain, and an intracellular domain, and a CD3 zeta activating domain.

In some embodiments, the polynucleotide of the present invention encodes a TCR, wherein the TCR comprises an antigen binding molecule that specifically binds to BCMA, and wherein the TCR further comprises a fourth complementarity determining region (CDR4). In certain embodiments, the polynucleotide encodes a TCR, wherein the TCR comprises an antigen binding molecule that specifically binds to BCMA, and a constant region. In some embodiments, the constant region is selected from a constant region of IgG1, IgG2, IgG3, IgG4, IgA, IgD, IgE, and IgM.

III.A. Costimulatory Domain

In some embodiments, the polynucleotide of the present invention encodes a CAR, wherein the CAR comprises an antigen binding molecule that specifically binds to BCMA (one or more antigen binding molecules in Section II), and wherein the CAR further comprises a costimulatory domain. In some embodiments, the costimulatory domain is positioned between the antigen binding molecule and an activating domain. In certain embodiments, the costimulatory domain can comprise an extracellular domain, a transmembrane domain, and an intracellular signaling domain.

Extracellular Domain: In one embodiment, the extracellular domain comprises a hinge region (e.g., a spacer region). In another embodiment, the extracellular domain is from or derived from (e.g., comprises) CD28, CD28T, OX40, 4-1BB/CD137, CD2, CD3 (alpha, beta, delta, epsilon, gamma, zeta), CD4, CD5, CD7, CD8, CD9, CD16, CD22, CD27, CD30, CD 33, CD37, CD40, CD 45, CD64, CD80, CD86, CD134, CD137, CD154, programmed death-1 (PD-1), ICOS, April, BAFF, lymphocyte function-associated antigen-1 (LFA-1 (CD11a/CD18), CD247, CD276 (B7-H3), LIGHT (tumor necrosis factor superfamily member 14; TNFSF14), NKG2C, Ig alpha (CD79a), DAP-10, Fc gamma receptor, MHC class I molecule, TNFγ, integrin, signaling lymphocytic activation molecule, BTLA, Toll ligand receptor, ICAM-1, B7-H3, CDS, ICAM-1, GITR, BAFFR, LIGHT, HVEM (LIGHTR), KIRDS2, SLAMF7, NKp80 (KLRF1), NKp44, NKp30, NKp46, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, ITGAM, CD11b, ITGAX, CD11c, ITGB1, CD29, ITGB2, CD18, LFA-1, ITGB7, NKG2D, TNFR2, TRANCE/RANKL, DNAM1 (CD226), SLAMF4 (CD244, 2B4), CD84, CD96 (Tactile), CEACAM1, CRT AM, Ly9 (CD229), CD160 (BY55), PSGL1, CD100 (SEMA4D), CD69, SLAMF6 (NTB-A, Ly108), SLAM (SLAMF1, CD150, IPO-3), BLAME (SLAMF8), SELPLG (CD162), LTBR, LAT, GADS, SLP-76, PAG/Cbp, CD19a, CD83 ligand, or fragments or combinations thereof. The extracellular domain can be derived either from a natural or from a synthetic source.

In some embodiments, the extracellular domain in the costimulatory domain is positioned between the antigen binding molecule and the transmembrane domain. In certain embodiments, the extracellular domain in the costimulatory domain is from or derived from an immunoglobulin. In some embodiments, the extracellular domain in the costimulatory domain is selected from the hinge regions of IgG1, IgG2, IgG3, IgG4, IgA, IgD, IgE, and IgM, or a fragment thereof. In other embodiments, the extracellular domain in the costimulatory domain is from or derived from the hinge region of CD8 alpha. In one particular embodiment, the extracellular domain in the costimulatory domain is from or derived from the hinge region of CD28. In certain embodiments, the extracellular domain in the costimulatory domain comprises a fragment of the hinge region of CD8 alpha or a fragment of the hinge region of CD28, wherein the fragment is anything less than the whole hinge region. In some embodiments, the fragment of the CD8 alpha hinge region or the fragment of the CD28 hinge region comprises an amino acid sequence that excludes at least 1, at least 2, at least 3, at least 4, at least 5, at least 6, at least 7, at least 8, at least 9, at least 10, at least 11, at least 12, at least 13, at least 14, at least 15, at least 16, at least 17, at least 18, at least 19, or at least 20 amino acids at the N-terminus or C-Terminus, or both, of the CD8 alpha hinge region of the CD28 hinge region.

In certain embodiments, the extracellular domain in the costimulatory domain comprises an amino acid sequence that is at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to the amino acid sequence LDNEKSNGTIIHVKGKHLCPSPLFPGPSKP (SEQ ID NO: 167) or a fragment thereof. In some embodiments, the extracellular domain in the costimulatory domain comprises the amino acid sequence of SEQ ID NO: 167 or a fragment thereof.

In certain embodiments, the extracellular domain in the costimulatory domain is encoded by a nucleotide sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to the nucleotide sequence CTTGATAATGAAAAGTCAAACGGAACAATCATT CACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCA (SEQ ID NO: 166) or a fragment thereof. In some embodiments, the extracellular domain in the costimulatory domain is encoded by a nucleotide sequence that comprises the nucleotide sequence of SEQ ID NO: 166 or a fragment thereof.

In some embodiments, the CD28T domain is derived from a human CD28 hinge region. In other embodiments, the CD28T domain is derived from a rodent, murine, or primate (e.g., non-human primate) CD28 hinge region. In some embodiments, the CD28T domain is derived from a chimeric CD28 hinge region.

In some embodiments, the extracellular domain comprises some or all of a member of the immunoglobulin family such as IgG1, IgG2, IgG3, IgG4, IgA, IgD, IgE, IgM, or fragment thereof.

Transmembrane Domain: The costimulatory domain for the CAR or TCR of the invention can further comprise a transmembrane domain. The transmembrane domain can be designed to be fused to the extracellular domain in the costimulatory domain. It can similarly be fused to the intracellular domain in the costimulatory domain. In one embodiment, the transmembrane domain that naturally is associated with one of the domains in a CAR is used. In some instances, the transmembrane domain can be selected or modified by amino acid substitution to avoid binding of such domains to the transmembrane domains of the same or different surface membrane proteins to minimize interactions with other members of the receptor complex. The transmembrane domain may be derived either from a natural or from a synthetic source. Where the source is natural, the domain can be derived from any membrane-bound or transmembrane protein. In some embodiments, the transmembrane domain is derived from CD28, OX-40, 4-1BB/CD137, CD2, CD3 (alpha, beta, delta, epsilon, zeta), CD4, CD5, CD7, CD8, CD9, CD16, CD22, CD27, CD30, CD 33, CD37, CD40, CD 45, CD64, CD80, CD86, CD134, CD137, CD154, programmed death-1 (PD-1), ICOS, lymphocyte function-associated antigen-1 (LFA-1 (CD11a/CD18), CD3 gamma, CD247, CD276 (B7-H3), LIGHT (tumor necrosis factor superfamily member 14; TNFSF14), NKG2C, Ig alpha (CD79a), DAP-10, Fc gamma receptor, MHC class I molecule, TNFγ, integrin, signaling lymphocytic activation molecule, BTLA, Toll ligand receptor, ICAM-1, B7-H3, CDS, ICAM-1, GITR, BAFFR, LIGHT, HVEM (LIGHTR), KIRDS2, SLAMF7, NKp80 (KLRF1), NKp44, NKp30, NKp46, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, ITGAM, CD11b, ITGAX, CD11c, ITGB1, CD29, ITGB2, CD18, LFA-1, ITGB7, NKG2D, TNFR2, TRANCE/RANKL, DNAM1 (CD226), SLAMF4 (CD244, 2B4), CD84, CD96 (Tactile), CEACAM1, CRT AM, Ly9 (CD229), CD160 (BY55), PSGL1, CD100 (SEMA4D), CD69, SLAMF6 (NTB-A, Ly108), SLAM (SLAMF1, CD150, IPO-3), BLAME (SLAMF8), SELPLG (CD162), LTBR, LAT, GADS, SLP-76, PAG/Cbp, CD19a, CD83 ligand, or a fragment thereof.

Optionally, a short oligo or polypeptide linker, preferably between 2 and 10 amino acids in length may form the linkage between the transmembrane domain and the cytoplasmic signaling domain of the CAR. A glycine-serine doublet provides a particularly suitable linker.

In one embodiment, the transmembrane domain in the CAR of the invention comprises the CD8 transmembrane domain. In one embodiment, the CD8 transmembrane domain comprises the transmembrane portion of the nucleic acid sequence of GCTGCAGCATTGAGCAACTCAATAATGTATTTTAGTCACTTTGTACCAGTGTTCTTGCCGGC TAAGCCTACTACCACACCCGCTCCACGGCCACCTACCCCAGCTCCTACCATCGCTTCACAGC CTCTGTCCCTGCGCCCAGAGGCTTGCCGACCGGCCGCAGGGGGCGCTGTTCATACCAGAGGA CTGGATTTCGCCTGCGATATCTATATCTGGGCACCCCTGGCCGGAACCTGCGGCGTACTCCT GCTGTCCCTGGTCATCACGCTCTATTGTAATCACAGGAAC (SEQ ID NO: 269). In one embodiment, the CD8 transmembrane domain comprises the nucleic acid sequence that encodes the transmembrane amino acid sequence contained within

(SEQ ID NO: 270) AAALSNSIMYFSHEVPVFLPAKPTTTPAPRPPTPAPTIASQPLSLRPEA CRPAAGGAVHTRGLDFACDIYIWAPLAGTCGVLLLSLVITLYCNHRN.

In another embodiment, the transmembrane domain in the costimulating domain is a CD28 transmembrane domain. In some embodiments, the transmembrane domain comprises an amino acid sequence that is at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to the amino acid sequence FWVLVVVGGVLACYSLLVTVAFIIFWV (SEQ ID NO: 169). In some embodiments, the transmembrane domain comprises the amino acid sequence of SEQ ID NO: 169.

In some embodiments, the transmembrane domain is encoded by a nucleotide sequence at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to the nucleotide sequence TTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGC TTTTATAATCTTCTGGGTT (SEQ ID NO: 168). In some embodiments, the transmembrane domain is encoded by a nucleotide sequence that comprises the nucleotide sequence of SEQ ID NO: 168.

Intracellular (signaling) Domain: The intracellular (signaling) domain of the engineered T cells of the invention can provide signaling to an activating domain, which then activates at least one of the normal effector functions of the immune cell. Effector function of a T cell, for example, can be cytolytic activity or helper activity including the secretion of cytokines.

In certain embodiments, suitable intracellular signaling domain include (i.e., comprise), but are not limited to CD28, CD28T, OX-40, 4-1BB/CD137, CD2, CD7, CD27, CD30, CD40, programmed death-1 (PD-1), inducible T cell costimulator (ICOS), lymphocyte function-associated antigen-1 (LFA-1, CD11a/CD18), CD3 gamma, CD3 delta, CD3 epsilon, CD247, CD276 (B7-H3), LIGHT, (TNFSF14), NKG2C, Ig alpha (CD79a), DAP-10, Fc gamma receptor, MHC class 1 molecule, TNF receptor proteins, an Immunoglobulin protein, cytokine receptor, integrins, Signaling Lymphocytic Activation Molecules (SLAM proteins), activating NK cell receptors, BTLA, a Toll ligand receptor, ICAM-1, B7-H3, CDS, ICAM-1, GITR, BAFFR, LIGHT, HVEM (LIGHTR), KIRDS2, SLAMF7, NKp80 (KLRF1), NKp44, NKp30, NKp46, CD19, CD4, CD8alpha, CD8beta, IL-2R beta, IL-2R gamma, IL-7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, ITGAM, CD11b, ITGAX, CD11c, ITGB1, CD29, ITGB2, CD18, LFA-1, ITGB7, NKG2D, TNFR2, TRANCE/RANKL, DNAM1 (CD226), SLAMF4 (CD244, 2B4), CD84, CD96 (Tactile), CEACAM1, CRT AM, Ly9 (CD229), CD160 (BY55), PSGL1, CD100 (SEMA4D), CD69, SLAMF6 (NTB-A, Ly108), SLAM (SLAMF1, CD150, IPO-3), BLAME (SLAMF8), SELPLG (CD162), LTBR, LAT, GADS, SLP-76, PAG/Cbp, CD19a, a ligand that specifically binds with CD83, or any combination thereof.

An example of a nucleotide sequence encoding the intracellular signaling domain is set forth in SEQ ID NO. 170:

AGATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTC CACGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACGCACCACC TAGAGATTTCGCTGCCTATCGGAGC.

In one embodiment, the polynucleotide encoding an intracellular signaling domain within a costimulatory domain comprises a nucleotide sequence at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or about 100% identical to the nucleotide sequence of SEQ ID NO: 170.

An example of an intracellular signaling domain is set forth in SEQ ID NO. 171:

RSKRSRLLHSDYMNMTPRRPGPTRKHYQPYAPPRDFAAYRS

In one particular embodiment, the intracellular signaling domain within a costimulatory domain comprises an amino acid sequence at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or about 100% identical to the amino acid sequence of SEQ ID NO: 171.

The intracellular signaling sequences within the CAR of the invention can be linked to each other or to an activating domain in a random or specified order. Optionally, a short oligo- or polypeptide linker, preferably between 2 and 10 amino acids in length may form the linkage. A glycine-serine doublet provides a particularly suitable linker.

It will further be appreciated that where desired, the costimulatory regions described herein can be expressed in a separate chain from the antigen binding molecule (e.g., scFv) and activating domains, in so-called “trans” configuration.

III.B Activating Domain

In some embodiments, intracellular domains for use in the engineered T cell of the invention include cytoplasmic sequences of the T cell receptor (TCR) and co-receptors that act in concert to initiate signal transduction following antigen/receptor engagement, as well as any derivative or variant of these sequences and any synthetic sequence that has the same functional capability. CD3 is an element of the T cell receptor on native T cells, and has been shown to be an important intracellular activating element in CARs. In one embodiment, the activating domain is CD3, e.g., CD3 zeta, the nucleotide sequence of which is set forth in SEQ ID NO. 172:

AGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCC AGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGAAGAGTATGA CGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCA AGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATA AGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAG GGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAG GATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG.

In some embodiments, the polynucleotide encoding an activating domain comprises a nucleotide sequence at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or about 100% identical to the nucleotide sequence of SEQ ID NO: 172.

The corresponding amino acid of intracellular CD3 zeta is set forth in SEQ ID NO. 173:

RVKFSRSADAPAYQQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKP RRKNPQEGLYNELQK  DKMAEAYSEIGMKGERRRGKGHDGLYQGLSTATKDTYDALHMQALPPR.

In some embodiments, the activating domain comprises an amino acid sequence at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or about 100% identical to the amino acid sequence of SEQ ID NO: 173.

Additionally, in certain embodiments the activating domain comprises an amino acid sequence at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or about 100% identical to the amino acid sequence of a CD3 zeta variant as set forth in SEQ ID NO: 412:

RVKFSRSADAPAYKQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKP RRKNPQEGLYNELQKDKMAEAYSEIGMKGERRRGKGHDGLYQGLSTATK DTYDALHMQALPPR.

III.C. Leader Peptide

In some embodiments, the polynucleotide of the present invention encodes a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA, and wherein the CAR or the TCR further comprises a leader peptide (also referred to herein as a “signal peptide”). In certain embodiments, the leader peptide comprises an amino acid sequence that is at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to the amino acid sequence MALPVTALLLPLALLLHAARP (SEQ ID NO: 165). In some embodiments, the signal peptide comprises the amino acid sequence of SEQ ID NO: 165. In some embodiments, the leader peptide is encoded by a nucleotide sequence at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or about 100% identical to SEQ ID NO: 164.

In some embodiments, the polynucleotide of the present invention encodes a CAR, wherein the CAR comprises a leader peptide (P), an antigen binding molecule (B), a hinge domain (H), a transmembrane domain (T), a costimulatory region (C), and an activation domain (A), wherein the CAR is configured according to the following: P-B-H-T-C-A. In some embodiments, the antigen binding molecule comprises a VH and a VL, wherein the CAR is configured according to the following: P-VH-VL-H-T-C-A or P-VL-VH-H-T-C-A. In some embodiments, the VH and the VL are connected by a linker (L), wherein the anti-BCMA CAR is configured according to the following, from N-terminus to C-terminus: P-VH-L-VL-H-T-C-A or P-VH-L-VL-H-T-C-A.

In some embodiments, the polynucleotide of the present invention encodes a CAR, wherein the CAR comprises an amino acid sequence at least about 75%, at least about 85%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from Table 2. In certain embodiments, the polynucleotide of the present invention encodes a CAR, wherein the CAR comprises an amino acid sequence selected from Table 2.

TABLE 2 Example CAR Sequences SEQ SEQ Anti- ID ID BCMA CAR Nucleotide Sequence NO: Amino Acid Sequence NO: FS- ATGGCACTCCCCGTAACTGCTCTGCTGC 175 MALPVTALLLPLALLLHAARP 176 21495CAR TGCCGTTGGCATTGCTCCTGCACGCCGC EVQLLESGGGLVQPGGSLRLS HxL ACGCCCGGAGGTGCAGCTGTTGGAGTCT CAASGFTFSSYAMSWVRQAPG GGGGGAGGCTTGGTACAGCCTGGGGGGT KGLEWVSAISGSGGSTYYADS CCCTGAGACTCTCCTGTGCAGCCTCTGG VKGRFTISRDNSKNTLYLQMN ATTCACCTTTAGCAGCTATGCCATGAGC SLRAEDTAVYYCARAEMGAVF TGGGTCCGCCAGGCTCCAGGGAAGGGGC DIWGQGTMVTVSSGSTSGSGK TGGAGTGGGTCTCAGCTATTAGTGGTAG PGSGEGSTKGEIVLTQSPATL TGGTGGTAGCACATACTACGCAGACTCC SLSPGERATLSCRASQSVSRY GTGAAGGGCCGGTTCACCATCTCCAGAG LAWYQQKPGQAPRLLIYDASN ACAATTCCAAGAACACGCTGTATCTGCA RATGIPARFSGSGSGTDFTLT AATGAACAGCCTGAGAGCCGAGGACACG ISSLEPEDFAVYYCQQRISWP GCGGTGTACTACTGCGCAAGAGCCGAGA FTFGGGTKVEIKRAAALDNEK TGGGAGCCGTATTCGACATATGGGGTCA SNGTIIHVKGKHLCPSPLFPG GGGTACAATGGTCACCGTCTCCTCAGGG PSKPFWVLVVVGGVLACYSLL TCTACATCCGGCTCCGGGAAGCCCGGAA VTVAFIIFWVRSKRSRLLHSD GTGGCGAAGGTAGTACAAAGGGGGAAAT YMNMTPRRPGPTRKHYQPYAP TGTGTTGACACAGTCTCCAGCCACCCTG PRDFAAYRSRVKFSRSADAPA TCTTTGTCTCCAGGGGAAAGAGCCACCC YQQGQNQLYNELNLGRREEYD TCTCCTGCAGGGCCAGTCAGAGTGTTAG VLDKRRGRDPEMGGKPRRKNP CAGGTACTTAGCCTGGTACCAACAGAAA QEGLYNELQKDKMAEAYSEIG CCTGGCCAGGCTCCCAGGCTCCTCATCT MKGERRRGKGHDGLYQGLSTA ATGATGCATCCAACAGGGCCACTGGCAT TKDTYDALHMQALPPR CCCAGCCAGGTTCAGTGGCAGTGGGTCT GGGACAGACTTCACTCTCACCATCAGCA GCCTAGAGCCTGAAGATTTTGCAGTTTA TTACTGTCAGCAGAGAATCTCCTGGCCT TTCACTTTTGGCGGAGGGACCAAGGTTG AGATCAAACGGGCCGCTGCCCTTGATAA TGAAAAGTCAAACGGAACAATCATTCAC GTGAAGGGCAAGCACCTCTGTCCGTCAC CCTTGTTCCCTGGTCCATCCAAGCCATT CTGGGTGTTGGTCGTAGTGGGTGGAGTC CTCGCTTGTTACTCTCTGCTCGTCACCG TGGCTTTTATAATCTTCTGGGTTAGATC CAAAAGAAGCCGCCTGCTCCATAGCGAT TACATGAATATGACTCCACGCCGCCCTG GCCCCACAAGGAAACACTACCAGCCTTA CGCACCACCTAGAGATTTCGCTGCCTAT CGGAGCAGGGTGAAGTTTTCCAGATCTG CAGATGCACCAGCGTATCAGCAGGGCCA GAACCAACTGTATAACGAGCTCAACCTG GGACGCAGGGAAGAGTATGACGTTTTGG ACAAGCGCAGAGGACGGGACCCTGAGAT GGGTGGCAAACCAAGACGAAAAAACCCC CAGGAGGGTCTCTATAATGAGCTGCAGA AGGATAAGATGGCTGAAGCCTATTCTGA AATAGGCATGAAAGGAGAGCGGAGAAGG GGAAAAGGGCACGACGGTTTGTACCAGG GACTCAGCACTGCTACGAAGGATACTTA TGACGCTCTCCACATGCAAGCCCTGCCA CCTAGGTAA FS- ATGGCACTCCCCGTAACTGCTCTGCTGC 177 MALPVTALLLPLALLLHAARP 178 21495CAR TGCCGTTGGCATTGCTCCTGCACGCCGC EIVLTQSPATLSLSPGERATL LxH ACGCCCGGAAATTGTGTTGACACAGTCT SCRASQSVSRYLAWYQQKPGQ CCAGCCACCCTGTCTTTGTCTCCAGGGG APRLLIYDASNRATGIPARES AAAGAGCCACCCTCTCCTGCAGGGCCAG GSGSGTDFTLTISSLEPEDFA TCAGAGTGTTAGCAGGTACTTAGCCTGG VYYCQQRISWPFTFGGGTKVE TACCAACAGAAACCTGGCCAGGCTCCCA IKRGSTSGSGKPGSGEGSTKG GGCTCCTCATCTATGATGCATCCAACAG EVQLLESGGGLVQPGGSLRLS GGCCACTGGCATCCCAGCCAGGTTCAGT CAASGFTFSSYAMSWVRQAPG GGCAGTGGGTCTGGGACAGACTTCACTC KGLEWVSAISGSGGSTYYADS TCACCATCAGCAGCCTAGAGCCTGAAGA VKGRFTISRDNSKNTLYLQMN TTTTGCAGTTTATTACTGTCAGCAGAGA SLRAEDTAVYYCARAEMGAVF ATCTCCTGGCCTTTCACTTTTGGCGGAG DIWGQGTMVTVSSAAALDNEK GGACCAAGGTTGAGATCAAACGGGGGTC SNGTIIHVKGKHLCPSPLFPG TACATCCGGCTCCGGGAAGCCCGGAAGT PSKPFWVLVVVGGVLACYSLL GGCGAAGGTAGTACAAAGGGGGAGGTGC VTVAFIIFWVRSKRSRLLHSD AGCTGTTGGAGTCTGGGGGAGGCTTGGT YMNMTPRRPGPTRKHYQPYAP ACAGCCTGGGGGGTCCCTGAGACTCTCC PRDFAAYRSRVKFSRSADAPA TGTGCAGCCTCTGGATTCACCTTTAGCA YQQGQNQLYNELNLGRREEYD GCTATGCCATGAGCTGGGTCCGCCAGGC VLDKRRGRDPEMGGKPRRKNP TCCAGGGAAGGGGCTGGAGTGGGTCTCA QEGLYNELQKDKMAEAYSEIG GCTATTAGTGGTAGTGGTGGTAGCACAT MKGERRRGKGHDGLYQGLSTA ACTACGCAGACTCCGTGAAGGGCCGGTT TKDTYDALHMQALPPR CACCATCTCCAGAGACAATTCCAAGAAC ACGCTGTATCTGCAAATGAACAGCCTGA GAGCCGAGGACACGGCGGTGTACTACTG CGCAAGAGCCGAGATGGGAGCCGTATTC GACATATGGGGTCAGGGTACAATGGTCA CCGTCTCCTCAGCCGCTGCCCTTGATAA TGAAAAGTCAAACGGAACAATCATTCAC GTGAAGGGCAAGCACCTCTGTCCGTCAC CCTTGTTCCCTGGTCCATCCAAGCCATT CTGGGTGTTGGTCGTAGTGGGTGGAGTC CTCGCTTGTTACTCTCTGCTCGTCACCG TGGCTTTTATAATCTTCTGGGTTAGATC CAAAAGAAGCCGCCTGCTCCATAGCGAT TACATGAATATGACTCCACGCCGCCCTG GCCCCACAAGGAAACACTACCAGCCTTA CGCACCACCTAGAGATTTCGCTGCCTAT CGGAGCAGGGTGAAGTTTTCCAGATCTG CAGATGCACCAGCGTATCAGCAGGGCCA GAACCAACTGTATAACGAGCTCAACCTG GGACGCAGGGAAGAGTATGACGTTTTGG ACAAGCGCAGAGGACGGGACCCTGAGAT GGGTGGCAAACCAAGACGAAAAAACCCC CAGGAGGGTCTCTATAATGAGCTGCAGA AGGATAAGATGGCTGAAGCCTATTCTGA AATAGGCATGAAAGGAGAGCGGAGAAGG GGAAAAGGGCACGACGGTTTGTACCAGG GACTCAGCACTGCTACGAAGGATACTTA TGACGCTCTCCACATGCAAGCCCTGCCA CCTAGGTAA PC- ATGGCACTCCCCGTAACTGCTCTGCTGC 179 MALPVTALLLPLALLLHAARP 180 21497CAR TGCCGTTGGCATTGCTCCTGCACGCCGC QVQLVESGGGVVQPGRSLRLS HxL ACGCCCGCAGGTGCAGCTGGTGGAGTCT CAASGFTFSSYGMHWVRQAPG GGGGGAGGCGTGGTCCAGCCTGGGAGGT KGLEWVAVISYDGSNKYYADS CCCTGAGACTCTCCTGTGCAGCGTCTGG VKGRFTISRDNSKNTLYLQMN ATTCACCTTCAGTAGCTATGGCATGCAC SLRAEDTAVYYCARDGTYLGG TGGGTCCGCCAGGCTCCAGGCAAGGGGC LWYFDLWGRGTLVTVSSGSTS TGGAGTGGGTGGCAGTTATATCGTATGA GSGKPGSGEGSTKGDIVMTQS TGGAAGTAATAAATACTATGCAGACTCC PLSLPVTPGEPASISCRSSQS GTGAAGGGCCGATTCACCATCTCCAGAG LLHSNGYNYLDWYLQKPGQSP ACAATTCCAAGAACACGCTGTATCTGCA QLLIYLGSNRASGVPDRFSGS AATGAACAGCCTGAGAGCCGAGGACACG GSGTDFTLKISRVEAEDVGVY GCGGTGTACTACTGCGCCAGAGACGGTA YCMQGLGLPLTFGGGTKVEIK CTTATCTAGGTGGTCTCTGGTACTTCGA RAAALDNEKSNGTIIHVKGKH CTTATGGGGGAGAGGTACCTTGGTCACC LCPSPLFPGPSKPFWVLVVVG GTCTCCTCAGGGTCTACATCCGGCTCCG GVLACYSLLVTVAFIIFWVRS GGAAGCCCGGAAGTGGCGAAGGTAGTAC KRSRLLHSDYMNMTPRRPGPT AAAGGGGGATATTGTGATGACTCAGTCT RKHYQPYAPPRDFAAYRSRVK CCACTCTCCCTGCCCGTCACCCCTGGAG FSRSADAPAYQQGQNQLYNEL AGCCGGCCTCCATCTCCTGCAGGTCTAG NLGRREEYDVLDKRRGRDPEM TCAGAGCCTCCTGCATAGTAATGGATAC GGKPRRKNPQEGLYNELQKDK AACTATTTGGATTGGTACCTGCAGAAGC MAEAYSEIGMKGERRRGKGHD CAGGGCAGTCTCCACAGCTCCTGATCTA GLYQGLSTATKDTYDALHMQA TTTGGGTTCTAATCGGGCCTCCGGGGTC LPPR CCTGACAGGTTCAGTGGCAGTGGATCAG GCACAGATTTTACACTGAAAATCAGCAG AGTGGAGGCTGAGGATGTTGGGGTTTAT TACTGCATGCAGGGACTCGGCCTCCCTC TCACTTTTGGCGGAGGGACCAAGGTTGA GATCAAACGGGCCGCTGCCCTTGATAAT GAAAAGTCAAACGGAACAATCATTCACG TGAAGGGCAAGCACCTCTGTCCGTCACC CTTGTTCCCTGGTCCATCCAAGCCATTC TGGGTGTTGGTCGTAGTGGGTGGAGTCC TCGCTTGTTACTCTCTGCTCGTCACCGT GGCTTTTATAATCTTCTGGGTTAGATCC AAAAGAAGCCGCCTGCTCCATAGCGATT ACATGAATATGACTCCACGCCGCCCTGG CCCCACAAGGAAACACTACCAGCCTTAC GCACCACCTAGAGATTTCGCTGCCTATC GGAGCAGGGTGAAGTTTTCCAGATCTGC AGATGCACCAGCGTATCAGCAGGGCCAG AACCAACTGTATAACGAGCTCAACCTGG GACGCAGGGAAGAGTATGACGTTTTGGA CAAGCGCAGAGGACGGGACCCTGAGATG GGTGGCAAACCAAGACGAAAAAACCCCC AGGAGGGTCTCTATAATGAGCTGCAGAA GGATAAGATGGCTGAAGCCTATTCTGAA ATAGGCATGAAAGGAGAGCGGAGAAGGG GAAAAGGGCACGACGGTTTGTACCAGGG ACTCAGCACTGCTACGAAGGATACTTAT GACGCTCTCCACATGCAAGCCCTGCCAC CTAGGTAA PC- ATGGCACTCCCCGTAACTGCTCTGCTGC 181 MALPVTALLLPLALLLHAARP 182 21497CAR TGCCGTTGGCATTGCTCCTGCACGCCGC DIVMTQSPLSLPVTPGEPASI HxL ACGCCCGGATATTGTGATGACTCAGTCT SCRSSQSLLHSNGYNYLDWYL CCACTCTCCCTGCCCGTCACCCCTGGAG QKPGQSPQLLIYLGSNRASGV AGCCGGCCTCCATCTCCTGCAGGTCTAG PDRFSGSGSGTDFTLKISRVE TCAGAGCCTCCTGCATAGTAATGGATAC AEDVGVYYCMQGLGLPLTFGG AACTATTTGGATTGGTACCTGCAGAAGC GTKVEIKRGSTSGSGKPGSGE CAGGGCAGTCTCCACAGCTCCTGATCTA GSTKGQVQLVESGGGVVQPGR TTTGGGTTCTAATCGGGCCTCCGGGGTC SLRLSCAASGFTFSSYGMHWV CCTGACAGGTTCAGTGGCAGTGGATCAG RQAPGKGLEWVAVISYDGSNK GCACAGATTTTACACTGAAAATCAGCAG YYADSVKGRFTISRDNSKNTL AGTGGAGGCTGAGGATGTTGGGGTTTAT YLQMNSLRAEDTAVYYCARDG TACTGCATGCAGGGACTCGGCCTCCCTC TYLGGLWYFDLWGRGTLVTVS TCACTTTTGGCGGAGGGACCAAGGTTGA SAAALDNEKSNGTIIHVKGKH GATCAAACGGGGGTCTACATCCGGCTCC LCPSPLFPGPSKPFWVLVVVG GGGAAGCCCGGAAGTGGCGAAGGTAGTA GVLACYSLLVTVAFIIFWVRS CAAAGGGGCAGGTGCAGCTGGTGGAGTC KRSRLLHSDYMNMTPRRPGPT TGGGGGAGGCGTGGTCCAGCCTGGGAGG RKHYQPYAPPRDFAAYRSRVK TCCCTGAGACTCTCCTGTGCAGCGTCTG FSRSADAPAYQQGQNQLYNEL GATTCACCTTCAGTAGCTATGGCATGCA NLGRREEYDVLDKRRGRDPEM CTGGGTCCGCCAGGCTCCAGGCAAGGGG GGKPRRKNPQEGLYNELQKDK CTGGAGTGGGTGGCAGTTATATCGTATG MAEAYSEIGMKGERRRGKGHD ATGGAAGTAATAAATACTATGCAGACTC GLYQGLSTATKDTYDALHMQA CGTGAAGGGCCGATTCACCATCTCCAGA LPPR GACAATTCCAAGAACACGCTGTATCTGC AAATGAACAGCCTGAGAGCCGAGGACAC GGCGGTGTACTACTGCGCCAGAGACGGT ACTTATCTAGGTGGTCTCTGGTACTTCG ACTTATGGGGGAGAGGTACCTTGGTCAC CGTCTCCTCAGCCGCTGCCCTTGATAAT GAAAAGTCAAACGGAACAATCATTCACG TGAAGGGCAAGCACCTCTGTCCGTCACC CTTGTTCCCTGGTCCATCCAAGCCATTC TGGGTGTTGGTCGTAGTGGGTGGAGTCC TCGCTTGTTACTCTCTGCTCGTCACCGT GGCTTTTATAATCTTCTGGGTTAGATCC AAAAGAAGCCGCCTGCTCCATAGCGATT ACATGAATATGACTCCACGCCGCCCTGG CCCCACAAGGAAACACTACCAGCCTTAC GCACCACCTAGAGATTTCGCTGCCTATC GGAGCAGGGTGAAGTTTTCCAGATCTGC AGATGCACCAGCGTATCAGCAGGGCCAG AACCAACTGTATAACGAGCTCAACCTGG GACGCAGGGAAGAGTATGACGTTTTGGA CAAGCGCAGAGGACGGGACCCTGAGATG GGTGGCAAACCAAGACGAAAAAACCCCC AGGAGGGTCTCTATAATGAGCTGCAGAA GGATAAGATGGCTGAAGCCTATTCTGAA ATAGGCATGAAAGGAGAGCGGAGAAGGG GAAAAGGGCACGACGGTTTGTACCAGGG ACTCAGCACTGCTACGAAGGATACTTAT GACGCTCTCCACATGCAAGCCCTGCCAC CTAGGTAA AJ- ATGGCACTCCCCGTAACTGCTCTGCTGC 183 MALPVTALLLPLALLLHAARP 184 21508CAR TGCCGTTGGCATTGCTCCTGCACGCCGC QVQLVQSGAEVKKPGASVKVS HxL ACGCCCGCAGGTGCAGCTGGTGCAGTCT CKASGYTFTSYYMHWVRQAPG GGGGCTGAGGTGAAGAAGCCTGGGGCCT QGLEWMGIINPGGGSTSYAQK CAGTGAAGGTTTCCTGCAAGGCATCTGG FQGRVTMTRDTSTSTVYMELS ATACACCTTCACCAGCTACTATATGCAC SLRSEDTAVYYCARESWPMDV TGGGTGCGACAGGCCCCTGGACAAGGGC WGQGTTVTVSSGSTSGSGKPG TTGAGTGGATGGGAATAATCAACCCTGG SGEGSTKGEIVMTQSPATLSV TGGTGGTAGCACAAGCTACGCACAGAAG SPGERATLSCRASQSVSSNLA TTCCAGGGCAGAGTCACCATGACCAGGG WYQQKPGQAPRLLIYGASTRA ACACGTCCACGAGCACAGTCTACATGGA TGIPARFSGSGSGTEFTLTIS GCTGAGCAGCCTGAGATCTGAGGACACG SLQSEDFAVYYCQQYAAYPTF GCGGTGTACTACTGCGCCAGAGAGAGTT GGGTKVEIKRAAALDNEKSNG GGCCAATGGACGTATGGGGCCAGGGAAC TIIHVKGKHLCPSPLFPGPSK AACTGTCACCGTCTCCTCAGGGTCTACA PFWVLVVVGGVLACYSLLVTV TCCGGCTCCGGGAAGCCCGGAAGTGGCG AFIIFWVRSKRSRLLHSDYMN AAGGTAGTACAAAGGGGGAAATAGTGAT MTPRRPGPTRKHYQPYAPPRD GACGCAGTCTCCAGCCACCCTGTCTGTG FAAYRSRVKFSRSADAPAYQQ TCTCCAGGGGAAAGAGCCACCCTCTCCT GQNQLYNELNLGRREEYDVLD GCAGGGCCAGTCAGAGTGTTAGCAGCAA KRRGRDPEMGGKPRRKNPQEG CTTAGCCTGGTACCAGCAGAAACCTGGC LYNELQKDKMAEAYSEIGMKG CAGGCTCCCAGGCTCCTCATCTATGGTG ERRRGKGHDGLYQGLSTATKD CATCCACCAGGGCCACTGGTATCCCAGC TYDALHMQALPPR CAGGTTCAGTGGCAGTGGGTCTGGGACA GAGTTCACTCTCACCATCAGCAGCCTGC AGTCTGAAGATTTTGCAGTTTATTACTG TCAGCAGTACGCCGCCTACCCTACTTTT GGCGGAGGGACCAAGGTTGAGATCAAAC GGGCCGCTGCCCTTGATAATGAAAAGTC AAACGGAACAATCATTCACGTGAAGGGC AAGCACCTCTGTCCGTCACCCTTGTTCC CTGGTCCATCCAAGCCATTCTGGGTGTT GGTCGTAGTGGGTGGAGTCCTCGCTTGT TACTCTCTGCTCGTCACCGTGGCTTTTA TAATCTTCTGGGTTAGATCCAAAAGAAG CCGCCTGCTCCATAGCGATTACATGAAT ATGACTCCACGCCGCCCTGGCCCCACAA GGAAACACTACCAGCCTTACGCACCACC TAGAGATTTCGCTGCCTATCGGAGCAGG GTGAAGTTTTCCAGATCTGCAGATGCAC CAGCGTATCAGCAGGGCCAGAACCAACT GTATAACGAGCTCAACCTGGGACGCAGG GAAGAGTATGACGTTTTGGACAAGCGCA GAGGACGGGACCCTGAGATGGGTGGCAA ACCAAGACGAAAAAACCCCCAGGAGGGT CTCTATAATGAGCTGCAGAAGGATAAGA TGGCTGAAGCCTATTCTGAAATAGGCAT GAAAGGAGAGCGGAGAAGGGGAAAAGGG CACGACGGTTTGTACCAGGGACTCAGCA CTGCTACGAAGGATACTTATGACGCTCT CCACATGCAAGCCCTGCCACCTAGGTAA AJ- ATGGCACTCCCCGTAACTGCTCTGCTGC 185 MALPVTALLLPLALLLHAARP 186 21508CAR TGCCGTTGGCATTGCTCCTGCACGCCGC EIVMTQSPATLSVSPGERATL LxH ACGCCCGGAAATAGTGATGACGCAGTCT SCRASQSVSSNLAWYQQKPGQ CCAGCCACCCTGTCTGTGTCTCCAGGGG APRLLIYGASTRATGIPARFS AAAGAGCCACCCTCTCCTGCAGGGCCAG GSGSGTEFTLTISSLQSEDFA TCAGAGTGTTAGCAGCAACTTAGCCTGG VYYCQQYAAYPTFGGGTKVEI TACCAGCAGAAACCTGGCCAGGCTCCCA KRGSTSGSGKPGSGEGSTKGQ GGCTCCTCATCTATGGTGCATCCACCAG VQLVQSGAEVKKPGASVKVSC GGCCACTGGTATCCCAGCCAGGTTCAGT KASGYTFTSYYMHWVRQAPGQ GGCAGTGGGTCTGGGACAGAGTTCACTC GLEWMGIINPGGGSTSYAQKF TCACCATCAGCAGCCTGCAGTCTGAAGA QGRVTMTRDTSTSTVYMELSS TTTTGCAGTTTATTACTGTCAGCAGTAC LRSEDTAVYYCARESWPMDVW GCCGCCTACCCTACTTTTGGCGGAGGGA GQGTTVTVSSAAALDNEKSNG CCAAGGTTGAGATCAAACGGGGGTCTAC TIIHVKGKHLCPSPLFPGPSK ATCCGGCTCCGGGAAGCCCGGAAGTGGC PFWVLVVVGGVLACYSLLVTV GAAGGTAGTACAAAGGGGCAGGTGCAGC AFIIFWVRSKRSRLLHSDYMN TGGTGCAGTCTGGGGCTGAGGTGAAGAA MTPRRPGPTRKHYQPYAPPRD GCCTGGGGCCTCAGTGAAGGTTTCCTGC FAAYRSRVKFSRSADAPAYQQ AAGGCATCTGGATACACCTTCACCAGCT GQNQLYNELNLGRREEYDVLD ACTATATGCACTGGGTGCGACAGGCCCC KRRGRDPEMGGKPRRKNPQEG TGGACAAGGGCTTGAGTGGATGGGAATA LYNELQKDKMAEAYSEIGMKG ATCAACCCTGGTGGTGGTAGCACAAGCT ERRRGKGHDGLYQGLSTATKD ACGCACAGAAGTTCCAGGGCAGAGTCAC TYDALHMQALPPR CATGACCAGGGACACGTCCACGAGCACA GTCTACATGGAGCTGAGCAGCCTGAGAT CTGAGGACACGGCGGTGTACTACTGCGC CAGAGAGAGTTGGCCAATGGACGTATGG GGCCAGGGAACAACTGTCACCGTCTCCT CAGCCGCTGCCCTTGATAATGAAAAGTC AAACGGAACAATCATTCACGTGAAGGGC AAGCACCTCTGTCCGTCACCCTTGTTCC CTGGTCCATCCAAGCCATTCTGGGTGTT GGTCGTAGTGGGTGGAGTCCTCGCTTGT TACTCTCTGCTCGTCACCGTGGCTTTTA TAATCTTCTGGGTTAGATCCAAAAGAAG CCGCCTGCTCCATAGCGATTACATGAAT ATGACTCCACGCCGCCCTGGCCCCACAA GGAAACACTACCAGCCTTACGCACCACC TAGAGATTTCGCTGCCTATCGGAGCAGG GTGAAGTTTTCCAGATCTGCAGATGCAC CAGCGTATCAGCAGGGCCAGAACCAACT GTATAACGAGCTCAACCTGGGACGCAGG GAAGAGTATGACGTTTTGGACAAGCGCA GAGGACGGGACCCTGAGATGGGTGGCAA ACCAAGACGAAAAAACCCCCAGGAGGGT CTCTATAATGAGCTGCAGAAGGATAAGA TGGCTGAAGCCTATTCTGAAATAGGCAT GAAAGGAGAGCGGAGAAGGGGAAAAGGG CACGACGGTTTGTACCAGGGACTCAGCA CTGCTACGAAGGATACTTATGACGCTCT CCACATGCAAGCCCTGCCACCTAGGTAA NM- ATGGCACTCCCCGTAACTGCTCTGCTGC 187 MALPVTALLLPLALLLHAARP 188 21517CAR TGCCGTTGGCATTGCTCCTGCACGCCGC QLQLQESGPGLVKPSETLSLT HxL ACGCCCGCAGCTGCAGCTGCAGGAGTCG CTVSGGSISSSSYYWGWIRQP GGCCCAGGACTGGTGAAGCCTTCGGAGA PGKGLEWIGSISYSGSTYYNP CCCTGTCCCTCACCTGCACTGTCTCTGG SLKSRVTISVDTSKNQFSLKL TGGCTCCATCAGCAGTAGTAGTTACTAC SSVTAADTAVYYCARGRGYAT TGGGGCTGGATCCGCCAGCCCCCAGGGA SLAFDIWGQGTMVTVSSGSTS AGGGGCTGGAGTGGATTGGGAGTATCTC GSGKPGSGEGSTKGEIVLTQS CTATAGTGGGAGCACCTACTACAACCCG PATLSLSPGERATLSCRASQS TCCCTCAAGAGTCGAGTCACCATATCCG VSSYLAWYQQKPGQAPRLLIY TAGACACGTCCAAGAACCAGTTCTCCCT DASNRATGIPARFSGSGSGTD GAAGCTGAGTTCTGTGACCGCCGCAGAC FTLTISSLEPEDFAVYYCQQR ACGGCGGTGTACTACTGCGCCAGAGGCA HVWPPTFGGGTKVEIKRAAAL GGGGATATGCAACCAGCTTAGCCTTCGA DNEKSNGTIIHVKGKHLCPSP TATCTGGGGTCAGGGTACAATGGTCACC LFPGPSKPFWVLVVVGGVLAC GTCTCCTCAGGGTCTACATCCGGCTCCG YSLLVTVAFIIFWVRSKRSRL GGAAGCCCGGAAGTGGCGAAGGTAGTAC LHSDYMNMTPRRPGPTRKHYQ AAAGGGGGAAATTGTGTTGACACAGTCT PYAPPRDFAAYRSRVKFSRSA CCAGCCACCCTGTCTTTGTCTCCAGGGG DAPAYQQGQNQLYNELNLGRR AAAGAGCCACCCTCTCCTGCAGGGCCAG EEYDVLDKRRGRDPEMGGKPR TCAGAGTGTTAGCAGCTACTTAGCCTGG RKNPQEGLYNELQKDKMAEAY TACCAACAGAAACCTGGCCAGGCTCCCA SEIGMKGERRRGKGHDGLYQG GGCTCCTCATCTATGATGCATCCAACAG LSTATKDTYDALHMQALPPR GGCCACTGGCATCCCAGCCAGGTTCAGT GGCAGTGGGTCTGGGACAGACTTCACTC TCACCATCAGCAGCCTAGAGCCTGAAGA TTTTGCAGTTTATTACTGTCAGCAGAGA CACGTCTGGCCTCCTACTTTTGGCGGAG GGACCAAGGTTGAGATCAAACGGGCCGC TGCCCTTGATAATGAAAAGTCAAACGGA ACAATCATTCACGTGAAGGGCAAGCACC TCTGTCCGTCACCCTTGTTCCCTGGTCC ATCCAAGCCATTCTGGGTGTTGGTCGTA GTGGGTGGAGTCCTCGCTTGTTACTCTC TGCTCGTCACCGTGGCTTTTATAATCTT CTGGGTTAGATCCAAAAGAAGCCGCCTG CTCCATAGCGATTACATGAATATGACTC CACGCCGCCCTGGCCCCACAAGGAAACA CTACCAGCCTTACGCACCACCTAGAGAT TTCGCTGCCTATCGGAGCAGGGTGAAGT TTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAAC GAGCTCAACCTGGGACGCAGGGAAGAGT ATGACGTTTTGGACAAGCGCAGAGGACG GGACCCTGAGATGGGTGGCAAACCAAGA CGAAAAAACCCCCAGGAGGGTCTCTATA ATGAGCTGCAGAAGGATAAGATGGCTGA AGCCTATTCTGAAATAGGCATGAAAGGA GAGCGGAGAAGGGGAAAAGGGCACGACG GTTTGTACCAGGGACTCAGCACTGCTAC GAAGGATACTTATGACGCTCTCCACATG CAAGCCCTGCCACCTAGGTAA NM- ATGGCACTCCCCGTAACTGCTCTGCTGC 189 MALPVTALLLPLALLLHAARP 190 21517CAR TGCCGTTGGCATTGCTCCTGCACGCCGC EIVLTQSPATLSLSPGERATL LxH ACGCCCGGAAATTGTGTTGACACAGTCT SCRASQSVSSYLAWYQQKPGQ CCAGCCACCCTGTCTTTGTCTCCAGGGG APRLLIYDASNRATGIPARES AAAGAGCCACCCTCTCCTGCAGGGCCAG GSGSGTDFTLTISSLEPEDFA TCAGAGTGTTAGCAGCTACTTAGCCTGG VYYCQQRHVWPPTFGGGTKVE TACCAACAGAAACCTGGCCAGGCTCCCA IKRGSTSGSGKPGSGEGSTKG GGCTCCTCATCTATGATGCATCCAACAG QLQLQESGPGLVKPSETLSLT GGCCACTGGCATCCCAGCCAGGTTCAGT CTVSGGSISSSSYYWGWIRQP GGCAGTGGGTCTGGGACAGACTTCACTC PGKGLEWIGSISYSGSTYYNP TCACCATCAGCAGCCTAGAGCCTGAAGA SLKSRVTISVDTSKNQFSLKL TTTTGCAGTTTATTACTGTCAGCAGAGA SSVTAADTAVYYCARGRGYAT CACGTCTGGCCTCCTACTTTTGGCGGAG SLAFDIWGQGTMVTVSSAAAL GGACCAAGGTTGAGATCAAACGGGGGTC DNEKSNGTIIHVKGKHLCPSP TACATCCGGCTCCGGGAAGCCCGGAAGT LFPGPSKPFWVLVVVGGVLAC GGCGAAGGTAGTACAAAGGGGCAGCTGC YSLLVTVAFIIFWVRSKRSRL AGCTGCAGGAGTCGGGCCCAGGACTGGT LHSDYMNMTPRRPGPTRKHYQ GAAGCCTTCGGAGACCCTGTCCCTCACC PYAPPRDFAAYRSRVKFSRSA TGCACTGTCTCTGGTGGCTCCATCAGCA DAPAYQQGQNQLYNELNLGRR GTAGTAGTTACTACTGGGGCTGGATCCG EEYDVLDKRRGRDPEMGGKPR CCAGCCCCCAGGGAAGGGGCTGGAGTGG RKNPQEGLYNELQKDKMAEAY ATTGGGAGTATCTCCTATAGTGGGAGCA SEIGMKGERRRGKGHDGLYQG CCTACTACAACCCGTCCCTCAAGAGTCG LSTATKDTYDALHMQALPPR AGTCACCATATCCGTAGACACGTCCAAG AACCAGTTCTCCCTGAAGCTGAGTTCTG TGACCGCCGCAGACACGGCGGTGTACTA CTGCGCCAGAGGCAGGGGATATGCAACC AGCTTAGCCTTCGATATCTGGGGTCAGG GTACAATGGTCACCGTCTCCTCAGCCGC TGCCCTTGATAATGAAAAGTCAAACGGA ACAATCATTCACGTGAAGGGCAAGCACC TCTGTCCGTCACCCTTGTTCCCTGGTCC ATCCAAGCCATTCTGGGTGTTGGTCGTA GTGGGTGGAGTCCTCGCTTGTTACTCTC TGCTCGTCACCGTGGCTTTTATAATCTT CTGGGTTAGATCCAAAAGAAGCCGCCTG CTCCATAGCGATTACATGAATATGACTC CACGCCGCCCTGGCCCCACAAGGAAACA CTACCAGCCTTACGCACCACCTAGAGAT TTCGCTGCCTATCGGAGCAGGGTGAAGT TTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAAC GAGCTCAACCTGGGACGCAGGGAAGAGT ATGACGTTTTGGACAAGCGCAGAGGACG GGACCCTGAGATGGGTGGCAAACCAAGA CGAAAAAACCCCCAGGAGGGTCTCTATA ATGAGCTGCAGAAGGATAAGATGGCTGA AGCCTATTCTGAAATAGGCATGAAAGGA GAGCGGAGAAGGGGAAAAGGGCACGACG GTTTGTACCAGGGACTCAGCACTGCTAC GAAGGATACTTATGACGCTCTCCACATG CAAGCCCTGCCACCTAGGTAA TS- ATGGCACTCCCCGTAACTGCTCTGCTGC 191 MALPVTALLLPLALLLHAARP 192 21522CAR TGCCGTTGGCATTGCTCCTGCACGCCGC EVQLVESGGGLVQPGGSLRLS HxL ACGCCCGGAGGTGCAGCTGGTGGAGTCT CAASGFTFSSYSMNWVRQAPG GGGGGAGGCTTGGTACAGCCTGGGGGGT KGLEWVSTISSSSSTIYYADS CCCTGAGACTCTCCTGTGCAGCCTCTGG VKGRFTISRDNAKNSLYLQMN ATTCACCTTCAGTAGCTATAGCATGAAC SLRAEDTAVYYCARGSQEHLI TGGGTCCGCCAGGCTCCAGGGAAGGGGC FDYWGQGTLVTVSSGSTSGSG TGGAGTGGGTTTCAACCATTAGTAGTAG KPGSGEGSTKGEIVLTQSPAT TAGTAGTACCATATACTACGCAGACTCT LSLSPGERATLSCRASQSVSR GTGAAGGGCCGATTCACCATCTCCAGAG YLAWYQQKPGQAPRLLIYDAS ACAATGCCAAGAACTCACTGTATCTGCA NRATGIPARFSGSGSGTDFTL AATGAACAGCCTGAGAGCTGAGGACACG TISSLEPEDFAVYYCQQRFYY GCGGTGTACTACTGCGCCAGAGGTTCTC PWTFGGGTKVEIKRAAALDNE AGGAGCACCTGATTTTCGATTATTGGGG KSNGTIIHVKGKHLCPSPLFP ACAGGGTACATTGGTCACCGTCTCCTCA GPSKPFWVLVVVGGVLACYSL GGGTCTACATCCGGCTCCGGGAAGCCCG LVTVAFIIFWVRSKRSRLLHS GAAGTGGCGAAGGTAGTACAAAGGGGGA DYMNMTPRRPGPTRKHYQPYA AATTGTGTTGACACAGTCTCCAGCCACC PPRDFAAYRSRVKFSRSADAP CTGTCTTTGTCTCCAGGGGAAAGAGCCA AYQQGQNQLYNELNLGRREEY CCCTCTCCTGCAGGGCCAGTCAGAGTGT DVLDKRRGRDPEMGGKPRRKN TAGCAGGTACTTAGCCTGGTACCAACAG PQEGLYNELQKDKMAEAYSEI AAACCTGGCCAGGCTCCCAGGCTCCTCA GMKGERRRGKGHDGLYQGLST TCTATGATGCATCCAACAGGGCCACTGG ATKDTYDALHMQALPPR CATCCCAGCCAGGTTCAGTGGCAGTGGG TCTGGGACAGACTTCACTCTCACCATCA GCAGCCTAGAGCCTGAAGATTTTGCAGT TTATTACTGTCAGCAGAGATTCTACTAC CCTTGGACTTTTGGCGGAGGGACCAAGG TTGAGATCAAACGGGCCGCTGCCCTTGA TAATGAAAAGTCAAACGGAACAATCATT CACGTGAAGGGCAAGCACCTCTGTCCGT CACCCTTGTTCCCTGGTCCATCCAAGCC ATTCTGGGTGTTGGTCGTAGTGGGTGGA GTCCTCGCTTGTTACTCTCTGCTCGTCA CCGTGGCTTTTATAATCTTCTGGGTTAG ATCCAAAAGAAGCCGCCTGCTCCATAGC GATTACATGAATATGACTCCACGCCGCC CTGGCCCCACAAGGAAACACTACCAGCC TTACGCACCACCTAGAGATTTCGCTGCC TATCGGAGCAGGGTGAAGTTTTCCAGAT CTGCAGATGCACCAGCGTATCAGCAGGG CCAGAACCAACTGTATAACGAGCTCAAC CTGGGACGCAGGGAAGAGTATGACGTTT TGGACAAGCGCAGAGGACGGGACCCTGA GATGGGTGGCAAACCAAGACGAAAAAAC CCCCAGGAGGGTCTCTATAATGAGCTGC AGAAGGATAAGATGGCTGAAGCCTATTC TGAAATAGGCATGAAAGGAGAGCGGAGA AGGGGAAAAGGGCACGACGGTTTGTACC AGGGACTCAGCACTGCTACGAAGGATAC TTATGACGCTCTCCACATGCAAGCCCTG CCACCTAGGTAA TS- ATGGCACTCCCCGTAACTGCTCTGCTGC 193 MALPVTALLLPLALLLHAARP 194 21522CAR TGCCGTTGGCATTGCTCCTGCACGCCGC EIVLTQSPATLSLSPGERATL LxH ACGCCCGGAAATTGTGTTGACACAGTCT SCRASQSVSRYLAWYQQKPGQ CCAGCCACCCTGTCTTTGTCTCCAGGGG APRLLIYDASNRATGIPARES AAAGAGCCACCCTCTCCTGCAGGGCCAG GSGSGTDFTLTISSLEPEDFA TCAGAGTGTTAGCAGGTACTTAGCCTGG VYYCQQRFYYPWTFGGGTKVE TACCAACAGAAACCTGGCCAGGCTCCCA IKRGSTSGSGKPGSGEGSTKG GGCTCCTCATCTATGATGCATCCAACAG EVQLVESGGGLVQPGGSLRLS GGCCACTGGCATCCCAGCCAGGTTCAGT CAASGFTFSSYSMNWVRQAPG GGCAGTGGGTCTGGGACAGACTTCACTC KGLEWVSTISSSSSTIYYADS TCACCATCAGCAGCCTAGAGCCTGAAGA VKGRFTISRDNAKNSLYLQMN TTTTGCAGTTTATTACTGTCAGCAGAGA SLRAEDTAVYYCARGSQEHLI TTCTACTACCCTTGGACTTTTGGCGGAG FDYWGQGTLVTVSSAAALDNE GGACCAAGGTTGAGATCAAACGGGGGTC KSNGTIIHVKGKHLCPSPLFP TACATCCGGCTCCGGGAAGCCCGGAAGT GPSKPFWVLVVVGGVLACYSL GGCGAAGGTAGTACAAAGGGGGAGGTGC LVTVAFIIFWVRSKRSRLLHS AGCTGGTGGAGTCTGGGGGAGGCTTGGT DYMNMTPRRPGPTRKHYQPYA ACAGCCTGGGGGGTCCCTGAGACTCTCC PPRDFAAYRSRVKFSRSADAP TGTGCAGCCTCTGGATTCACCTTCAGTA AYQQGQNQLYNELNLGRREEY GCTATAGCATGAACTGGGTCCGCCAGGC DVLDKRRGRDPEMGGKPRRKN TCCAGGGAAGGGGCTGGAGTGGGTTTCA PQEGLYNELQKDKMAEAYSEI ACCATTAGTAGTAGTAGTAGTACCATAT GMKGERRRGKGHDGLYQGLST ACTACGCAGACTCTGTGAAGGGCCGATT ATKDTYDALHMQALPPR CACCATCTCCAGAGACAATGCCAAGAAC TCACTGTATCTGCAAATGAACAGCCTGA GAGCTGAGGACACGGCGGTGTACTACTG CGCCAGAGGTTCTCAGGAGCACCTGATT TTCGATTATTGGGGACAGGGTACATTGG TCACCGTCTCCTCAGCCGCTGCCCTTGA TAATGAAAAGTCAAACGGAACAATCATT CACGTGAAGGGCAAGCACCTCTGTCCGT CACCCTTGTTCCCTGGTCCATCCAAGCC ATTCTGGGTGTTGGTCGTAGTGGGTGGA GTCCTCGCTTGTTACTCTCTGCTCGTCA CCGTGGCTTTTATAATCTTCTGGGTTAG ATCCAAAAGAAGCCGCCTGCTCCATAGC GATTACATGAATATGACTCCACGCCGCC CTGGCCCCACAAGGAAACACTACCAGCC TTACGCACCACCTAGAGATTTCGCTGCC TATCGGAGCAGGGTGAAGTTTTCCAGAT CTGCAGATGCACCAGCGTATCAGCAGGG CCAGAACCAACTGTATAACGAGCTCAAC CTGGGACGCAGGGAAGAGTATGACGTTT TGGACAAGCGCAGAGGACGGGACCCTGA GATGGGTGGCAAACCAAGACGAAAAAAC CCCCAGGAGGGTCTCTATAATGAGCTGC AGAAGGATAAGATGGCTGAAGCCTATTC TGAAATAGGCATGAAAGGAGAGCGGAGA AGGGGAAAAGGGCACGACGGTTTGTACC AGGGACTCAGCACTGCTACGAAGGATAC TTATGACGCTCTCCACATGCAAGCCCTG CCACCTAGGTAA RY- ATGGCACTCCCCGTAACTGCTCTGCTGC 195 MALPVTALLLPLALLLHAARP 196 21527CAR TGCCGTTGGCATTGCTCCTGCACGCCGC QVQLVESGGGVVQPGRSLRLS HxL ACGCCCGCAGGTGCAGCTGGTGGAGTCT CAASGFTFSSYGMHWVRQAPG GGGGGAGGCGTGGTCCAGCCTGGGAGGT KGLEWVAVISYDGSNKYYADS CCCTGAGACTCTCCTGTGCAGCGTCTGG VKGRFTISRDNSKNTLYLQMN ATTCACCTTCAGTAGCTATGGCATGCAC SLRAEDTAVYYCARTDFWSGS TGGGTCCGCCAGGCTCCAGGCAAGGGGC PPGLDYWGQGTLVTVSSGSTS TGGAGTGGGTGGCAGTTATATCGTATGA GSGKPGSGEGSTKGDIQLTQS TGGAAGTAATAAATACTATGCAGACTCC PSSVSASVGDRVTITCRASQG GTGAAGGGCCGATTCACCATCTCCAGAG ISSWLAWYQQKPGKAPKLLIY ACAATTCCAAGAACACGCTGTATCTGCA GASSLQSGVPSRFSGSGSGTD AATGAACAGCCTGAGAGCCGAGGACACG FTLTISSLQPEDFATYYCQQI GCGGTGTACTACTGCGCCAGAACTGACT YTFPFTFGGGTKVEIKRAAAL TCTGGAGCGGATCCCCTCCAGGCTTAGA DNEKSNGTIIHVKGKHLCPSP TTACTGGGGACAGGGTACATTGGTCACC LFPGPSKPFWVLVVVGGVLAC GTCTCCTCAGGGTCTACATCCGGCTCCG YSLLVTVAFIIFWVRSKRSRL GGAAGCCCGGAAGTGGCGAAGGTAGTAC LHSDYMNMTPRRPGPTRKHYQ AAAGGGGGACATCCAGTTGACCCAGTCT PYAPPRDFAAYRSRVKFSRSA CCATCTTCCGTGTCTGCATCTGTAGGAG DAPAYQQGQNQLYNELNLGRR ACAGAGTCACCATCACTTGTCGGGCGAG EEYDVLDKRRGRDPEMGGKPR TCAGGGTATTAGCAGCTGGTTAGCCTGG RKNPQEGLYNELQKDKMAEAY TATCAGCAGAAACCAGGGAAAGCCCCTA SEIGMKGERRRGKGHDGLYQG AGCTCCTGATCTATGGTGCATCCAGTTT LSTATKDTYDALHMQALPPR GCAAAGTGGGGTCCCATCAAGGTTCAGC GGCAGTGGATCTGGGACAGATTTCACTC TCACCATCAGCAGCCTGCAGCCTGAAGA TTTTGCAACTTATTACTGTCAGCAGATA TACACCTTCCCTTTCACTTTTGGCGGAG GGACCAAGGTTGAGATCAAACGGGCCGC TGCCCTTGATAATGAAAAGTCAAACGGA ACAATCATTCACGTGAAGGGCAAGCACC TCTGTCCGTCACCCTTGTTCCCTGGTCC ATCCAAGCCATTCTGGGTGTTGGTCGTA GTGGGTGGAGTCCTCGCTTGTTACTCTC TGCTCGTCACCGTGGCTTTTATAATCTT CTGGGTTAGATCCAAAAGAAGCCGCCTG CTCCATAGCGATTACATGAATATGACTC CACGCCGCCCTGGCCCCACAAGGAAACA CTACCAGCCTTACGCACCACCTAGAGAT TTCGCTGCCTATCGGAGCAGGGTGAAGT TTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAAC GAGCTCAACCTGGGACGCAGGGAAGAGT ATGACGTTTTGGACAAGCGCAGAGGACG GGACCCTGAGATGGGTGGCAAACCAAGA CGAAAAAACCCCCAGGAGGGTCTCTATA ATGAGCTGCAGAAGGATAAGATGGCTGA AGCCTATTCTGAAATAGGCATGAAAGGA GAGCGGAGAAGGGGAAAAGGGCACGACG GTTTGTACCAGGGACTCAGCACTGCTAC GAAGGATACTTATGACGCTCTCCACATG CAAGCCCTGCCACCTAGGTAA RY- ATGGCACTCCCCGTAACTGCTCTGCTGC 197 MALPVTALLLPLALLLHAARP 198 21527CAR TGCCGTTGGCATTGCTCCTGCACGCCGC DIQLTQSPSSVSASVGDRVTI LxH ACGCCCGGACATCCAGTTGACCCAGTCT TCRASQGISSWLAWYQQKPGK CCATCTTCCGTGTCTGCATCTGTAGGAG APKLLIYGASSLQSGVPSRFS ACAGAGTCACCATCACTTGTCGGGCGAG GSGSGTDFTLTISSLQPEDFA TCAGGGTATTAGCAGCTGGTTAGCCTGG TYYCQQIYTFPFTFGGGTKVE TATCAGCAGAAACCAGGGAAAGCCCCTA IKRGSTSGSGKPGSGEGSTKG AGCTCCTGATCTATGGTGCATCCAGTTT QVQLVESGGGVVQPGRSLRLS GCAAAGTGGGGTCCCATCAAGGTTCAGC CAASGFTFSSYGMHWVRQAPG GGCAGTGGATCTGGGACAGATTTCACTC KGLEWVAVISYDGSNKYYADS TCACCATCAGCAGCCTGCAGCCTGAAGA VKGRFTISRDNSKNTLYLQMN TTTTGCAACTTATTACTGTCAGCAGATA SLRAEDTAVYYCARTDFWSGS TACACCTTCCCTTTCACTTTTGGCGGAG PPGLDYWGQGTLVTVSSAAAL GGACCAAGGTTGAGATCAAACGGGGGTC DNEKSNGTIIHVKGKHLCPSP TACATCCGGCTCCGGGAAGCCCGGAAGT LFPGPSKPFWVLVVVGGVLAC GGCGAAGGTAGTACAAAGGGGCAGGTGC YSLLVTVAFIIFWVRSKRSRL AGCTGGTGGAGTCTGGGGGAGGCGTGGT LHSDYMNMTPRRPGPTRKHYQ CCAGCCTGGGAGGTCCCTGAGACTCTCC PYAPPRDFAAYRSRVKFSRSA TGTGCAGCGTCTGGATTCACCTTCAGTA DAPAYQQGQNQLYNELNLGRR GCTATGGCATGCACTGGGTCCGCCAGGC EEYDVLDKRRGRDPEMGGKPR TCCAGGCAAGGGGCTGGAGTGGGTGGCA RKNPQEGLYNELQKDKMAEAY GTTATATCGTATGATGGAAGTAATAAAT SEIGMKGERRRGKGHDGLYQG ACTATGCAGACTCCGTGAAGGGCCGATT LSTATKDTYDALHMQALPPR CACCATCTCCAGAGACAATTCCAAGAAC ACGCTGTATCTGCAAATGAACAGCCTGA GAGCCGAGGACACGGCGGTGTACTACTG CGCCAGAACTGACTTCTGGAGCGGATCC CCTCCAGGCTTAGATTACTGGGGACAGG GTACATTGGTCACCGTCTCCTCAGCCGC TGCCCTTGATAATGAAAAGTCAAACGGA ACAATCATTCACGTGAAGGGCAAGCACC TCTGTCCGTCACCCTTGTTCCCTGGTCC ATCCAAGCCATTCTGGGTGTTGGTCGTA GTGGGTGGAGTCCTCGCTTGTTACTCTC TGCTCGTCACCGTGGCTTTTATAATCTT CTGGGTTAGATCCAAAAGAAGCCGCCTG CTCCATAGCGATTACATGAATATGACTC CACGCCGCCCTGGCCCCACAAGGAAACA CTACCAGCCTTACGCACCACCTAGAGAT TTCGCTGCCTATCGGAGCAGGGTGAAGT TTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAAC GAGCTCAACCTGGGACGCAGGGAAGAGT ATGACGTTTTGGACAAGCGCAGAGGACG GGACCCTGAGATGGGTGGCAAACCAAGA CGAAAAAACCCCCAGGAGGGTCTCTATA ATGAGCTGCAGAAGGATAAGATGGCTGA AGCCTATTCTGAAATAGGCATGAAAGGA GAGCGGAGAAGGGGAAAAGGGCACGACG GTTTGTACCAGGGACTCAGCACTGCTAC GAAGGATACTTATGACGCTCTCCACATG CAAGCCCTGCCACCTAGGTAA PP- ATGGCACTCCCCGTAACTGCTCTGCTGC 199 MALPVTALLLPLALLLHAARP 200 21528CAR TGCCGTTGGCATTGCTCCTGCACGCCGC QVQLVQSGAEVKKPGSSVKVS HxL ACGCCCGCAGGTGCAGCTGGTGCAGTCT CKASGGTFSSYAISWVRQAPG GGGGCTGAGGTGAAGAAGCCTGGGTCCT QGLEWMGGIIPIFGTANYAQK CGGTGAAGGTCTCCTGCAAGGCTTCTGG FQGRVTITADESTSTAYMELS AGGCACCTTCAGCAGCTATGCTATCAGC SLRSEDTAVYYCARTPEYSSS TGGGTGCGACAGGCCCCTGGACAAGGGC IWHYYYGMDVWGQGTTVTVSS TTGAGTGGATGGGAGGGATCATCCCTAT GSTSGSGKPGSGEGSTKGDIV CTTTGGTACAGCAAACTACGCACAGAAG MTQSPDSLAVSLGERATINCK TTCCAGGGCAGAGTCACGATTACCGCGG SSQSVLYSSNNKNYLAWYQQK ACGAATCCACGAGCACAGCCTACATGGA PGQPPKLLIYWASTRESGVPD GCTGAGCAGCCTGAGATCTGAGGACACG RFSGSGSGTDFTLTISSLQAE GCGGTGTACTACTGCGCCAGAACTCCTG DVAVYYCQQFAHTPFTFGGGT AATACTCCTCCAGCATATGGCACTATTA KVEIKRAAALDNEKSNGTIIH CTACGGCATGGACGTATGGGGCCAGGGA VKGKHLCPSPLFPGPSKPFWV ACAACTGTCACCGTCTCCTCAGGGTCTA LVVVGGVLACYSLLVTVAFII CATCCGGCTCCGGGAAGCCCGGAAGTGG FWVRSKRSRLLHSDYMNMTPR CGAAGGTAGTACAAAGGGGGACATCGTG RPGPTRKHYQPYAPPRDFAAY ATGACCCAGTCTCCAGACTCCCTGGCTG RSRVKFSRSADAPAYQQGQNQ TGTCTCTGGGCGAGAGGGCCACCATCAA LYNELNLGRREEYDVLDKRRG CTGCAAGTCCAGCCAGAGTGTTTTATAC RDPEMGGKPRRKNPQEGLYNE AGCTCCAACAATAAGAACTACTTAGCTT LQKDKMAEAYSEIGMKGERRR GGTACCAGCAGAAACCAGGACAGCCTCC GKGHDGLYQGLSTATKDTYDA TAAGCTGCTCATTTACTGGGCATCTACC LHMQALPPR CGGGAATCCGGGGTCCCTGACCGATTCA GTGGCAGCGGGTCTGGGACAGATTTCAC TCTCACCATCAGCAGCCTGCAGGCTGAA GATGTGGCAGTTTATTACTGTCAGCAGT TCGCCCACACTCCTTTCACTTTTGGCGG AGGGACCAAGGTTGAGATCAAACGGGCC GCTGCCCTTGATAATGAAAAGTCAAACG GAACAATCATTCACGTGAAGGGCAAGCA CCTCTGTCCGTCACCCTTGTTCCCTGGT CCATCCAAGCCATTCTGGGTGTTGGTCG TAGTGGGTGGAGTCCTCGCTTGTTACTC TCTGCTCGTCACCGTGGCTTTTATAATC TTCTGGGTTAGATCCAAAAGAAGCCGCC TGCTCCATAGCGATTACATGAATATGAC TCCACGCCGCCCTGGCCCCACAAGGAAA CACTACCAGCCTTACGCACCACCTAGAG ATTTCGCTGCCTATCGGAGCAGGGTGAA GTTTTCCAGATCTGCAGATGCACCAGCG TATCAGCAGGGCCAGAACCAACTGTATA ACGAGCTCAACCTGGGACGCAGGGAAGA GTATGACGTTTTGGACAAGCGCAGAGGA CGGGACCCTGAGATGGGTGGCAAACCAA GACGAAAAAACCCCCAGGAGGGTCTCTA TAATGAGCTGCAGAAGGATAAGATGGCT GAAGCCTATTCTGAAATAGGCATGAAAG GAGAGCGGAGAAGGGGAAAAGGGCACGA CGGTTTGTACCAGGGACTCAGCACTGCT ACGAAGGATACTTATGACGCTCTCCACA TGCAAGCCCTGCCACCTAGGTAA PP- ATGGCACTCCCCGTAACTGCTCTGCTGC 201 MALPVTALLLPLALLLHAARP 202 21528CAR TGCCGTTGGCATTGCTCCTGCACGCCGC DIVMTQSPDSLAVSLGERATI LxH ACGCCCGGACATCGTGATGACCCAGTCT NCKSSQSVLYSSNNKNYLAWY CCAGACTCCCTGGCTGTGTCTCTGGGCG QQKPGQPPKLLIYWASTRESG AGAGGGCCACCATCAACTGCAAGTCCAG VPDRFSGSGSGTDFTLTISSL CCAGAGTGTTTTATACAGCTCCAACAAT QAEDVAVYYCQQFAHTPFTFG AAGAACTACTTAGCTTGGTACCAGCAGA GGTKVEIKRGSTSGSGKPGSG AACCAGGACAGCCTCCTAAGCTGCTCAT EGSTKGQVQLVQSGAEVKKPG TTACTGGGCATCTACCCGGGAATCCGGG SSVKVSCKASGGTFSSYAISW GTCCCTGACCGATTCAGTGGCAGCGGGT VRQAPGQGLEWMGGIIPIFGT CTGGGACAGATTTCACTCTCACCATCAG ANYAQKFQGRVTITADESTST CAGCCTGCAGGCTGAAGATGTGGCAGTT AYMELSSLRSEDTAVYYCART TATTACTGTCAGCAGTTCGCCCACACTC PEYSSSIWHYYYGMDVWGQGT CTTTCACTTTTGGCGGAGGGACCAAGGT TVTVSSAAALDNEKSNGTIIH TGAGATCAAACGGGGGTCTACATCCGGC VKGKHLCPSPLFPGPSKPFWV TCCGGGAAGCCCGGAAGTGGCGAAGGTA LVVVGGVLACYSLLVTVAFII GTACAAAGGGGCAGGTGCAGCTGGTGCA FWVRSKRSRLLHSDYMNMTPR GTCTGGGGCTGAGGTGAAGAAGCCTGGG RPGPTRKHYQPYAPPRDFAAY TCCTCGGTGAAGGTCTCCTGCAAGGCTT RSRVKFSRSADAPAYQQGQNQ CTGGAGGCACCTTCAGCAGCTATGCTAT LYNELNLGRREEYDVLDKRRG CAGCTGGGTGCGACAGGCCCCTGGACAA RDPEMGGKPRRKNPQEGLYNE GGGCTTGAGTGGATGGGAGGGATCATCC LQKDKMAEAYSEIGMKGERRR CTATCTTTGGTACAGCAAACTACGCACA GKGHDGLYQGLSTATKDTYDA GAAGTTCCAGGGCAGAGTCACGATTACC LHMQALPPR GCGGACGAATCCACGAGCACAGCCTACA TGGAGCTGAGCAGCCTGAGATCTGAGGA CACGGCGGTGTACTACTGCGCCAGAACT CCTGAATACTCCTCCAGCATATGGCACT ATTACTACGGCATGGACGTATGGGGCCA GGGAACAACTGTCACCGTCTCCTCAGCC GCTGCCCTTGATAATGAAAAGTCAAACG GAACAATCATTCACGTGAAGGGCAAGCA CCTCTGTCCGTCACCCTTGTTCCCTGGT CCATCCAAGCCATTCTGGGTGTTGGTCG TAGTGGGTGGAGTCCTCGCTTGTTACTC TCTGCTCGTCACCGTGGCTTTTATAATC TTCTGGGTTAGATCCAAAAGAAGCCGCC TGCTCCATAGCGATTACATGAATATGAC TCCACGCCGCCCTGGCCCCACAAGGAAA CACTACCAGCCTTACGCACCACCTAGAG ATTTCGCTGCCTATCGGAGCAGGGTGAA GTTTTCCAGATCTGCAGATGCACCAGCG TATCAGCAGGGCCAGAACCAACTGTATA ACGAGCTCAACCTGGGACGCAGGGAAGA GTATGACGTTTTGGACAAGCGCAGAGGA CGGGACCCTGAGATGGGTGGCAAACCAA GACGAAAAAACCCCCAGGAGGGTCTCTA TAATGAGCTGCAGAAGGATAAGATGGCT GAAGCCTATTCTGAAATAGGCATGAAAG GAGAGCGGAGAAGGGGAAAAGGGCACGA CGGTTTGTACCAGGGACTCAGCACTGCT ACGAAGGATACTTATGACGCTCTCCACA TGCAAGCCCTGCCACCTAGGTAA RD- ATGGCACTCCCCGTAACTGCTCTGCTGC 203 MALPVTALLLPLALLLHAARP 204 21530CAR TGCCGTTGGCATTGCTCCTGCACGCCGC QVQLVESGGGVVQPGRSLRLS HxL ACGCCCGCAGGTGCAGCTGGTGGAGTCT CAASGFTFSSYGMHWVRQAPG GGGGGAGGCGTGGTCCAGCCTGGGAGGT KGLEWVAVISYDGSNKYYADS CCCTGAGACTCTCCTGTGCAGCGTCTGG VKGRFTISRDNSKNTLYLQMN ATTCACCTTCAGTAGCTATGGCATGCAC SLRAEDTAVYYCVKGPLQEPP TGGGTCCGCCAGGCTCCAGGCAAGGGGC YDYGMDVWGQGTTVTVSSGST TGGAGTGGGTGGCAGTTATATCGTATGA SGSGKPGSGEGSTKGEIVMTQ TGGAAGTAATAAATACTATGCAGACTCC SPATLSVSPGERATLSCRASQ GTGAAGGGCCGATTCACCATCTCCAGAG SVSSNLAWYQQKPGQAPRLLI ACAATTCCAAGAACACGCTGTATCTGCA YSASTRATGIPARFSGSGSGT AATGAACAGCCTGAGAGCCGAGGACACG EFTLTISSLQSEDFAVYYCQQ GCGGTGTACTACTGCGTCAAGGGGCCGT HHVWPLTFGGGTKVEIKRAAA TGCAGGAGCCGCCATACGATTATGGAAT LDNEKSNGTIIHVKGKHLCPS GGACGTATGGGGCCAGGGAACAACTGTC PLFPGPSKPFWVLVVVGGVLA ACCGTCTCCTCAGGGTCTACATCCGGCT CYSLLVTVAFIIFWVRSKRSR CCGGGAAGCCCGGAAGTGGCGAAGGTAG LLHSDYMNMTPRRPGPTRKHY TACAAAGGGGGAAATAGTGATGACGCAG QPYAPPRDFAAYRSRVKFSRS TCTCCAGCCACCCTGTCTGTGTCTCCAG ADAPAYQQGQNQLYNELNLGR GGGAAAGAGCCACCCTCTCCTGCAGGGC REEYDVLDKRRGRDPEMGGKP CAGTCAGAGTGTTAGCAGCAACTTAGCC RRKNPQEGLYNELQKDKMAEA TGGTACCAGCAGAAACCTGGCCAGGCTC YSEIGMKGERRRGKGHDGLYQ CCAGGCTCCTCATCTATAGCGCATCCAC GLSTATKDTYDALHMQALPPR CAGGGCCACTGGTATCCCAGCCAGGTTC AGTGGCAGTGGGTCTGGGACAGAGTTCA CTCTCACCATCAGCAGCCTGCAGTCTGA AGATTTTGCAGTTTATTACTGTCAGCAG CACCACGTCTGGCCTCTCACTTTTGGCG GAGGGACCAAGGTTGAGATCAAACGGGC CGCTGCCCTTGATAATGAAAAGTCAAAC GGAACAATCATTCACGTGAAGGGCAAGC ACCTCTGTCCGTCACCCTTGTTCCCTGG TCCATCCAAGCCATTCTGGGTGTTGGTC GTAGTGGGTGGAGTCCTCGCTTGTTACT CTCTGCTCGTCACCGTGGCTTTTATAAT CTTCTGGGTTAGATCCAAAAGAAGCCGC CTGCTCCATAGCGATTACATGAATATGA CTCCACGCCGCCCTGGCCCCACAAGGAA ACACTACCAGCCTTACGCACCACCTAGA GATTTCGCTGCCTATCGGAGCAGGGTGA AGTTTTCCAGATCTGCAGATGCACCAGC GTATCAGCAGGGCCAGAACCAACTGTAT AACGAGCTCAACCTGGGACGCAGGGAAG AGTATGACGTTTTGGACAAGCGCAGAGG ACGGGACCCTGAGATGGGTGGCAAACCA AGACGAAAAAACCCCCAGGAGGGTCTCT ATAATGAGCTGCAGAAGGATAAGATGGC TGAAGCCTATTCTGAAATAGGCATGAAA GGAGAGCGGAGAAGGGGAAAAGGGCACG ACGGTTTGTACCAGGGACTCAGCACTGC TACGAAGGATACTTATGACGCTCTCCAC ATGCAAGCCCTGCCACCTAGGTAA RD- ATGGCACTCCCCGTAACTGCTCTGCTGC 205 MALPVTALLLPLALLLHAARP 206 21530CAR TGCCGTTGGCATTGCTCCTGCACGCCGC EIVMTQSPATLSVSPGERATL LxH ACGCCCGGAAATAGTGATGACGCAGTCT SCRASQSVSSNLAWYQQKPGQ CCAGCCACCCTGTCTGTGTCTCCAGGGG APRLLIYSASTRATGIPARFS AAAGAGCCACCCTCTCCTGCAGGGCCAG GSGSGTEFTLTISSLQSEDFA TCAGAGTGTTAGCAGCAACTTAGCCTGG VYYCQQHHVWPLTFGGGTKVE TACCAGCAGAAACCTGGCCAGGCTCCCA IKRGSTSGSGKPGSGEGSTKG GGCTCCTCATCTATAGCGCATCCACCAG QVQLVESGGGVVQPGRSLRLS GGCCACTGGTATCCCAGCCAGGTTCAGT CAASGFTFSSYGMHWVRQAPG GGCAGTGGGTCTGGGACAGAGTTCACTC KGLEWVAVISYDGSNKYYADS TCACCATCAGCAGCCTGCAGTCTGAAGA VKGRFTISRDNSKNTLYLQMN TTTTGCAGTTTATTACTGTCAGCAGCAC SLRAEDTAVYYCVKGPLQEPP CACGTCTGGCCTCTCACTTTTGGCGGAG YDYGMDVWGQGTTVTVSSAAA GGACCAAGGTTGAGATCAAACGGGGGTC LDNEKSNGTIIHVKGKHLCPS TACATCCGGCTCCGGGAAGCCCGGAAGT PLFPGPSKPFWVLVVVGGVLA GGCGAAGGTAGTACAAAGGGGCAGGTGC CYSLLVTVAFIIFWVRSKRSR AGCTGGTGGAGTCTGGGGGAGGCGTGGT LLHSDYMNMTPRRPGPTRKHY CCAGCCTGGGAGGTCCCTGAGACTCTCC QPYAPPRDFAAYRSRVKFSRS TGTGCAGCGTCTGGATTCACCTTCAGTA ADAPAYQQGQNQLYNELNLGR GCTATGGCATGCACTGGGTCCGCCAGGC REEYDVLDKRRGRDPEMGGKP TCCAGGCAAGGGGCTGGAGTGGGTGGCA RRKNPQEGLYNELQKDKMAEA GTTATATCGTATGATGGAAGTAATAAAT YSEIGMKGERRRGKGHDGLYQ ACTATGCAGACTCCGTGAAGGGCCGATT GLSTATKDTYDALHMQALPPR CACCATCTCCAGAGACAATTCCAAGAAC ACGCTGTATCTGCAAATGAACAGCCTGA GAGCCGAGGACACGGCGGTGTACTACTG CGTCAAGGGGCCGTTGCAGGAGCCGCCA TACGATTATGGAATGGACGTATGGGGCC AGGGAACAACTGTCACCGTCTCCTCAGC CGCTGCCCTTGATAATGAAAAGTCAAAC GGAACAATCATTCACGTGAAGGGCAAGC ACCTCTGTCCGTCACCCTTGTTCCCTGG TCCATCCAAGCCATTCTGGGTGTTGGTC GTAGTGGGTGGAGTCCTCGCTTGTTACT CTCTGCTCGTCACCGTGGCTTTTATAAT CTTCTGGGTTAGATCCAAAAGAAGCCGC CTGCTCCATAGCGATTACATGAATATGA CTCCACGCCGCCCTGGCCCCACAAGGAA ACACTACCAGCCTTACGCACCACCTAGA GATTTCGCTGCCTATCGGAGCAGGGTGA AGTTTTCCAGATCTGCAGATGCACCAGC GTATCAGCAGGGCCAGAACCAACTGTAT AACGAGCTCAACCTGGGACGCAGGGAAG AGTATGACGTTTTGGACAAGCGCAGAGG ACGGGACCCTGAGATGGGTGGCAAACCA AGACGAAAAAACCCCCAGGAGGGTCTCT ATAATGAGCTGCAGAAGGATAAGATGGC TGAAGCCTATTCTGAAATAGGCATGAAA GGAGAGCGGAGAAGGGGAAAAGGGCACG ACGGTTTGTACCAGGGACTCAGCACTGC TACGAAGGATACTTATGACGCTCTCCAC ATGCAAGCCCTGCCACCTAGGTAA

In some embodiments, the polynucleotide of the present invention encodes a CAR, wherein the CAR comprises an amino acid sequence at least about 75%, at least about 85%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, and 206. In certain embodiments, the CAR comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, and 206. In one embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 176. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 178. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 180. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 182. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 184. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 186. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 188. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 190. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 192. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 194. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 196. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 198. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 200. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 202. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 204. In another embodiment, the CAR comprises the amino acid sequence of SEQ ID NO: 206.

In some embodiments, the polynucleotide of the present invention comprises an nucleotide sequence at least about 50%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 85%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or 100% identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 175, 177, 179, 181, 183, 185, 187, 189, 191, 193, 195, 197, 199, 201, 203, and 205. In certain embodiments, the polynucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NOs: 175, 177, 179, 181, 183, 185, 187, 189, 191, 193, 195, 197, 199, 201, 203, and 205. In one embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 175. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 177. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 179. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 181. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 183. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 185. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 187. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 189. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 191. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 193. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 195. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 197. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 199. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 201. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 203. In another embodiment, the polynucleotide comprises the nucleotide sequence of SEQ ID NO: 205.

In further embodiments, the invention relates to Clone FS-26528 HC DNA (SEQ ID NO: 271) as follows:

GAGGTGCAGCTGTTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGT CCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACCTTTGACGACTATGC CATGGCATGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCA GCTATTAGTGATGCAGGTGACAGAACATACTACGCAGACTCCGTGAGGG GCCGGTTCACCATCTCCAGAGACAATTCCAAGAACACACTGTATCTGCA AATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCAAGA GCCGAGATGGGAGCCGTATTCGACATATGGGGTCAGGGTACAATGGTCA CCGTCTCCTCA.

In further embodiments, the invention relates to the Clone FS-26528 HC amino acid sequence (SEQ ID NO: 272):

EVQLLESGGG LVQPGGSLRL SCAASGFTFD DYAMAWVRQA PGKGLEWVSA ISDAGDRTYY ADSVRGRFTI SRDNSKNTLY LQMNSLRAED TAVYYCARAE MGAVFDIWGQ GTMVTVSS.

In further embodiments, the invention relates to HC CDR1 thereof: SCAASGFTFDDYAMA (SEQ ID NO: 273). In further embodiments, the invention relates to HC CDR2 thereof: AISDAGDRTYYADSVRG (SEQ ID NO: 274). In further embodiments, the invention relates to HC CDR3 thereof: ARAEMGAVFDI (SEQ ID NO: 275) [HC CDR3]

In further embodiments, the invention relates to Clone FS-26528 LC DNA (SEQ ID NO: 276):

GAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGG AAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGGTACTT AGCCTGGTACCAACAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTAT GATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTG GGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGA TTTTGCAGTTTATTACTGTCAGCAGAGAATCTCCTGGCCTTTCACTTTT GGCGGAGGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone FS-26528 LC AA sequence (SEQ ID NO: 277):

EIVLTQSPAT LSLSPGERAT LSCRASQSVS RYLAWYQQKP GQAPRLLIYD ASNRATGIPA RFSGSGSGTD FTLTISSLEP EDFAVYYCQQ RISWPFTFGG GTKVEIKR.

In further embodiments, the invention relates to LC CDR1 thereof: RASQSVSRYLA (SEQ ID NO: 278). In further embodiments, the invention relates to LC CDR2 thereof: DASNRAT (SEQ ID NO: 279). In further embodiments, the invention relates to the LC CDR3 thereof: QQRISWPFT (SEQ ID NO: 280).

In further embodiments, the invention relates to Clone FS-26528 CAR DNA H×L (SEQ ID NO: 281):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGGAGGTGCAGCTGTTGGAGTCTGGGGGAGGCTTGGT ACAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACC TTTGACGACTATGCCATGGCATGGGTCCGCCAGGCTCCAGGGAAGGGGC TGGAGTGGGTCTCAGCTATTAGTGATGCAGGTGACAGAACATACTACGC AGACTCCGTGAGGGGCCGGTTCACCATCTCCAGAGACAATTCCAAGAAC ACACTGTATCTGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGT ACTACTGCGCAAGAGCCGAGATGGGAGCCGTATTCGACATATGGGGTCA GGGTACAATGGTCACCGTCTCCTCAGGGTCTACATCCGGCTCCGGGAAG CCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATTGTGTTGACACAGT CTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTG CAGGGCCAGTCAGAGTGTTAGCAGGTACTTAGCCTGGTACCAACAGAAA CCTGGCCAGGCTCCCAGGCTCCTCATCTATGATGCATCCAACAGGGCCA CTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGACTTCAC TCTCACCATCAGCAGCCTAGAGCCTGAAGATTTTGCAGTTTATTACTGT CAGCAGAGAATCTCCTGGCCTTTCACTTTTGGCGGAGGGACCAAGGTTG AGATCAAACGGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAAT CATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGT CCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTT GTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATC CAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGC CGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAG ATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGC ACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTG GGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACC CTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTA TAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGC ATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGG GACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGC CCTGCCACCTAGG.

In further embodiments, the invention relates to Clone FS-26528 CAR H×L AA sequence (SEQ ID NO: 282):

MALPVTALLL PLALLLHAAR PEVQLLESGG GLVQPGGSLR LSCAASGFTF DDYAMAWVRQ APGKGLEWVS AISDAGDRTY YADSVRGRFT ISRDNSKNTL YLQMNSLRAE DTAVYYCARA EMGAVFDIWG QGTMVTVSSG STSGSGKPGS GEGSTKGEIV LTQSPATLSL SPGERATLSC RASQSVSRYL AWYQQKPGQA PRLLIYDASN RATGIPARFS GSGSGTDFTL TISSLEPEDF AVYYCQQRIS WPFTFGGGTK VEIKRAAALD NEKSNGTIIH VKGKHLCPSP LFPGPSKPFW VLVVVGGVLA CYSLLVTVAF IIFWVRSKRS RLLHSDYMNM TPRRPGPTRK HYQPYAPPRD FAAYRSRVKF SRSADAPAYQ QGQNQLYNEL NLGRREEYDV LDKRRGRDPE MGGKPRRKNP QEGLYNELQK DKMAEAYSEI GMKGERRRGK GHDGLYQGLS TATKDTYDAL HMQALPPR.

In further embodiments, the invention relates to Clone FS-26528 CAR DNA L×H (SEQ ID NO: 283):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGGAAATTGTGTTGACACAGTCTCCAGCCACCCTGTC TTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGT GTTAGCAGGTACTTAGCCTGGTACCAACAGAAACCTGGCCAGGCTCCCA GGCTCCTCATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAG GTTCAGTGGCAGTGGGTCTGGGACAGACTTCACTCTCACCATCAGCAGC CTAGAGCCTGAAGATTTTGCAGTTTATTACTGTCAGCAGAGAATCTCCT GGCCTTTCACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTC TACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGG GAGGTGCAGCTGTTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGT CCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACCTTTGACGACTATGC CATGGCATGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCA GCTATTAGTGATGCAGGTGACAGAACATACTACGCAGACTCCGTGAGGG GCCGGTTCACCATCTCCAGAGACAATTCCAAGAACACACTGTATCTGCA AATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCAAGA GCCGAGATGGGAGCCGTATTCGACATATGGGGTCAGGGTACAATGGTCA CCGTCTCCTCAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAAT CATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGT CCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTT GTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATC CAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGC CGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAG ATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGC ACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTG GGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACC CTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTA TAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGC ATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGG GACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGC CCTGCCACCTAGG.

In further embodiments, the invention relates to the Clone FS-26528 CAR L×H AA sequence (SEQ ID NO: 284):

MALPVTALLL PLALLLHAAR PEIVLTQSPA TLSLSPGERA TLSCRASQSV SRYLAWYQQK PGQAPRLLIY DASNRATGIP ARFSGSGSGT DFTLTISSLE PEDFAVYYCQ QRISWPFTFG GGTKVEIKRG STSGSGKPGS GEGSTKGEVQ LLESGGGLVQ PGGSLRLSCA ASGFTFDDYA MAWVRQAPGK GLEWVSAISD AGDRTYYADS VRGRFTISRD NSKNTLYLQM NSLRAEDTAV YYCARAEMGA VFDIWGQGTM VTVSSAAALD NEKSNGTIIH VKGKHLCPSP LFPGPSKPFW VLVVVGGVLA CYSLLVTVAF IIFWVRSKRS RLLHSDYMNM TPRRPGPTRK HYQPYAPPRD FAAYRSRVKF SRSADAPAYQ QGQNQLYNEL NLGRREEYDV LDKRRGRDPE MGGKPRRKNP QEGLYNELQK DKMAEAYSEI GMKGERRRGK GHDGLYQGLS TATKDTYDAL HMQALPPR.

In further embodiments, the invention relates to Clone PC-26534 HC DNA (SEQ ID NO: 285) as follows:

CAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGT CCCTGAGACTCTCCTGTGCAGCGTCTGGATTCACCTTCAGTGAGCATGG CATGCACTGGGTCCGCCAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCA GCTATATCTTATGATGGAAGGAATAAACACTATGCAGACTCCGTGAAGG GCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCA AATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCCAGA GACGGTACTTATCTAGGTGGTCTCTGGTACTTCGACTTATGGGGGAGAG GTACCTTGGTCACCGTCTCCTCA.

In further embodiments, the invention relates to Clone PC-26534 HC (SEQ ID NO: 286):

QVQLVESGGG VVQPGRSLRL SCAASGFTFS EHGMHWVRQA PGKGLEWVAA ISYDGRNKHY ADSVKGRFTI SRDNSKNTLY LQMNSLRAED TAVYYCARDG TYLGGLWYFD LWGRGTLVTV SS.

In further embodiments, the invention relates to HC CDR1 thereof: FTFSEHGMH (SEQ ID NO: 287). In further embodiments, the invention relates to HC CDR2 thereof: AISYDGRNKHYADSVKG (SEQ ID NO: 288). In further embodiments, the invention relates to HC CDR3 thereof: ARDGTYLGGLWYFDL (SEQ ID NO: 289).

In further embodiments, the invention relates to Clone PC-26534 LC DNA (SEQ ID NO: 290) as follows:

GATATTGTGATGACTCAGTCTCCACTCTCCCTGCCCGTCACCCCTGGAG AGCCGGCCTCCATCTCCTGCAGGTCTAGTCAGAGCCTCCTGCATAGTAA TGGATACAACTATTTGGATTGGTACCTGCAGAAGCCAGGGCAGTCTCCA CAGCTCCTGATCTATTTGGGTTCTAATCGGGCCTCCGGGGTCCCTGACA GGTTCAGTGGCAGTGGATCAGGCACAGATTTTACACTGAAAATCAGCAG AGTGGAGGCTGAGGATGTTGGGGTTTATTACTGCATGCAGGGACTCGGC CTCCCTCTCACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone PC-26534 LC AA sequence (SEQ ID NO: 291):

DIVMTQSPLS LPVTPGEPAS ISCRSSQSLL HSNGYNYLDW YLQKPGQSPQ LLIYLGSNRA SGVPDRFSGS GSGTDFTLKI SRVEAEDVGV YYCMQGLGLP LTFGGGTKVE IKR.

In further embodiments, the invention relates to LC CDR1 AA sequence thereof: RSSQSLLHSNGYNYLD (SEQ ID NO: 292). In further embodiments, the invention relates to LC CDR2 thereof: LGSNRAS (SEQ ID NO: 293). In further embodiments, the invention relates to LC CDR3 thereof: MQGLGLPLT (SEQ ID NO: 294).

In further embodiments, the invention relates to Clone PC-26534 CAR DNA H×L (SEQ ID NO: 295) as follows:

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGT CCAGCCTGGGAGGTCCCTGAGACTCTCCTGTGCAGCGTCTGGATTCACC TTCAGTGAGCATGGCATGCACTGGGTCCGCCAGGCTCCAGGCAAGGGGC TGGAGTGGGTGGCAGCTATATCTTATGATGGAAGGAATAAACACTATGC AGACTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAAC ACGCTGTATCTGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGT ACTACTGCGCCAGAGACGGTACTTATCTAGGTGGTCTCTGGTACTTCGA CTTATGGGGGAGAGGTACCTTGGTCACCGTCTCCTCAGGGTCTACATCC GGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGATATTG TGATGACTCAGTCTCCACTCTCCCTGCCCGTCACCCCTGGAGAGCCGGC CTCCATCTCCTGCAGGTCTAGTCAGAGCCTCCTGCATAGTAATGGATAC AACTATTTGGATTGGTACCTGCAGAAGCCAGGGCAGTCTCCACAGCTCC TGATCTATTTGGGTTCTAATCGGGCCTCCGGGGTCCCTGACAGGTTCAG TGGCAGTGGATCAGGCACAGATTTTACACTGAAAATCAGCAGAGTGGAG GCTGAGGATGTTGGGGTTTATTACTGCATGCAGGGACTCGGCCTCCCTC TCACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGCCGCTGCCCT TGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCAC CTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGT TGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGT GGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCAT AGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAAC ACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAG GGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAG AACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGAAGAGTATGACG TTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAG ACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAG ATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGG GAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGA TACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone PC-26534 CAR H×L AA sequence (SEQ ID NO: 296):

MALPVTALLL PLALLLHAAR PQVQLVESGG GVVQPGRSLR LSCAASGFTF SEHGMHWVRQ APGKGLEWVA AISYDGRNKH YADSVKGRFT ISRDNSKNTL YLQMNSLRAE DTAVYYCARD GTYLGGLWYF DLWGRGTLVT VSSGSTSGSG KPGSGEGSTK GDIVMTQSPL SLPVTPGEPA SISCRSSQSL LHSNGYNYLD WYLQKPGQSP QLLIYLGSNR ASGVPDRFSG SGSGTDFTLK ISRVEAEDVG VYYCMQGLGL PLTFGGGTKV EIKRAAALDN EKSNGTIIHV KGKHLCPSPL FPGPSKPFWV LVVVGGVLAC YSLLVTVAFI IFWVRSKRSR LLHSDYMNMT PRRPGPTRKH YQPYAPPRDF AAYRSRVKFS RSADAPAYQQ GQNQLYNELN LGRREEYDVL DKRRGRDPEM GGKPRRKNPQ EGLYNELQKD  KMAEAYSEIG MKGERRRGKG HDGLYQGLST ATKDTYDALH MQALPPR.

In further embodiments, the invention relates to Clone PC-26534 CAR DNA L×H (SEQ ID NO: 297):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGGATATTGTGATGACTCAGTCTCCACTCTCCCTGCC CGTCACCCCTGGAGAGCCGGCCTCCATCTCCTGCAGGTCTAGTCAGAGC CTCCTGCATAGTAATGGATACAACTATTTGGATTGGTACCTGCAGAAGC CAGGGCAGTCTCCACAGCTCCTGATCTATTTGGGTTCTAATCGGGCCTC CGGGGTCCCTGACAGGTTCAGTGGCAGTGGATCAGGCACAGATTTTACA CTGAAAATCAGCAGAGTGGAGGCTGAGGATGTTGGGGTTTATTACTGCA TGCAGGGACTCGGCCTCCCTCTCACTTTTGGCGGAGGGACCAAGGTTGA GATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAA GGTAGTACAAAGGGGCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGG TCCAGCCTGGGAGGTCCCTGAGACTCTCCTGTGCAGCGTCTGGATTCAC CTTCAGTGAGCATGGCATGCACTGGGTCCGCCAGGCTCCAGGCAAGGGG CTGGAGTGGGTGGCAGCTATATCTTATGATGGAAGGAATAAACACTATG CAGACTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAA CACGCTGTATCTGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTG TACTACTGCGCCAGAGACGGTACTTATCTAGGTGGTCTCTGGTACTTCG ACTTATGGGGGAGAGGTACCTTGGTCACCGTCTCCTCAGCCGCTGCCCT TGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCAC CTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGT TGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGT GGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCAT AGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAAC ACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAG GGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAG AACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGAAGAGTATGACG TTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAG ACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAG ATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGG GAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGA TACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone PC-26534 CAR L×H chain sequences (SEQ ID NO: 298):

MALPVTALLL PLALLLHAAR PDIVMTQSPL SLPVTPGEPA SISCRSSQSL LHSNGYNYLD WYLQKPGQSP QLLIYLGSNR ASGVPDRFSG SGSGTDFTLK ISRVEAEDVG VYYCMQGLGL PLTFGGGTKV EIKRGSTSGS GKPGSGEGST KGQVQLVESG GGVVQPGRSL RLSCAASGFT FSEHGMHWVR QAPGKGLEWV AAISYDGRNK HYADSVKGRF TISRDNSKNT LYLQMNSLRA EDTAVYYCAR DGTYLGGLWY FDLWGRGTLV TVSSAAALDN EKSNGTIIHV KGKHLCPSPL FPGPSKPFWV LVVVGGVLAC YSLLVTVAFI IFWVRSKRSR LLHSDYMNMT PRRPGPTRKH YQPYAPPRDF AAYRSRVKFS RSADAPAYQQ GQNQLYNELN LGRREEYDVL DKRRGRDPEM GGKPRRKNPQ EGLYNELQKD KMAEAYSEIG MKGERRRGKG HDGLYQGLST ATKDTYDALH MQALPPR.

In further embodiments, the invention relates to Clone AJ-26545 HC DNA (SEQ ID NO: 299):

CAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCT CAGTGAAGGTTTCCTGCAGGGCATCTGGATACACCTTCATGGAGCACTA TATGCACTGGGTGCGACAGGCCCCTGGACAAGGGCTTGAGTGGATGGGA GTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGCACAGAAGTTCCAGG GCAGAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGGA GCTGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGA GAGAATTGGCCAATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCT CCTCA.

In further embodiments, the invention relates to Clone AJ-26545 HC AA sequence (SEQ ID NO: 300):

QVQLVQSGAE VKKPGASVKV SCRASGYTFM EHYMHWVRQA PGQGLEWMGV IGPSGGKTSY AQKFQGRVTM TRDTSTSTVY MELSSLRSED TAVYYCARES WPMDVWGQGT TVTVSS.

In further embodiments, the invention relates to HC CDR1 thereof: YTFMEHYMH (SEQ ID NO: 301). In further embodiments, the invention relates to HC CDR2 thereof: VIGPSGGKTSYAQKFQG (SEQ ID NO: 302). In further embodiments, the invention relates to HC CDR3 thereof: ARESWPMDV (SEQ ID NO: 303).

In further embodiments, the invention relates to Clone AJ-26545 LC DNA (SEQ ID NO: 304):

GAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGG AAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTT AGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTAT GGTGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTCAGTGGCAGTG GGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGA TTTTGCAGTTTATTACTGTCAGCAGTACGCCGCCTACCCTACTTTTGGC GGAGGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone AJ-26545 LC AA sequence (SEQ ID NO: 305):

EIVMTQSPAT LSVSPGERAT LSCRASQSVS SNLAWYQQKP GQAPRLLIYG ASTRATGIPA RFSGSGSGTE FTLTISSLQS EDFAVYYCQQ YAAYPTFGGG TKVEIKR.

In further embodiments, the invention relates to LC CDR1 thereof: RASQSVSSNLA (SEQ ID NO: 306). In further embodiments, the invention relates to LC CDR2 thereof: GASTRAT (SEQ ID NO: 307). In further embodiments, the invention relates to the LC CDR3 thereof: QQYAAYPT (SEQ ID NO: 308).

In further embodiments, the invention relates to Clone AJ-26545 CAR DNA H×L (SEQ ID NO: 309):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAA GAAGCCTGGGGCCTCAGTGAAGGTTTCCTGCAGGGCATCTGGATACACC TTCATGGAGCACTATATGCACTGGGTGCGACAGGCCCCTGGACAAGGGC TTGAGTGGATGGGAGTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGC ACAGAAGTTCCAGGGCAGAGTCACCATGACCAGGGACACGTCCACGAGC ACAGTCTACATGGAGCTGAGCAGCCTGAGATCTGAGGACACGGCGGTGT ACTACTGCGCCAGAGAGAATTGGCCAATGGACGTATGGGGCCAGGGAAC AACTGTCACCGTCTCCTCAGGGTCTACATCCGGCTCCGGGAAGCCCGGA AGTGGCGAAGGTAGTACAAAGGGGGAAATAGTGATGACGCAGTCTCCAG CCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGC CAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGC CAGGCTCCCAGGCTCCTCATCTATGGTGCATCCACCAGGGCCACTGGTA TCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCAC CATCAGCAGCCTGCAGTCTGAAGATTTTGCAGTTTATTACTGTCAGCAG TACGCCGCCTACCCTACTTTTGGCGGAGGGACCAAGGTTGAGATCAAAC GGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGT GAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAG CCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTC TGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAG CCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGC CCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTG CCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGG GAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGG GTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCT GCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGA GAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCA CTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACC TAGG.

In further embodiments, the invention relates to Clone AJ-26545 CAR H×L AA sequence (SEQ ID NO: 310):

MALPVTALLL PLALLLHAAR PQVQLVQSGA EVKKPGASVK VSCRASGYTF MEHYMHWVRQ APGQGLEWMG VIGPSGGKTS YAQKFQGRVT MTRDTSTSTV YMELSSLRSE DTAVYYCARE SWPMDVWGQG TTVTVSSGST SGSGKPGSGE GSTKGEIVMT QSPATLSVSP GERATLSCRA SQSVSSNLAW YQQKPGQAPR LLIYGASTRA TGIPARFSGS GSGTEFTLTI SSLQSEDFAV YYCQQYAAYP TFGGGTKVEI KRAAALDNEK SNGTIIHVKG KHLCPSPLFP GPSKPFWVLV VVGGVLACYS LLVTVAFIIF WVRSKRSRLL HSDYMNMTPR RPGPTRKHYQ PYAPPRDFAA YRSRVKFSRS ADAPAYQQGQ NQLYNELNLG RREEYDVLDK RRGRDPEMGG KPRRKNPQEG LYNELQKDKM AEAYSEIGMK GERRRGKGHD GLYQGLSTAT KDTYDALHMQ ALPPR.

In further embodiments, the invention relates to Clone AJ-26545 CAR DNA L×H (SEQ ID NO: 311):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGGAAATAGTGATGACGCAGTCTCCAGCCACCCTGTC TGTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGT GTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCA GGCTCCTCATCTATGGTGCATCCACCAGGGCCACTGGTATCCCAGCCAG GTTCAGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGC CTGCAGTCTGAAGATTTTGCAGTTTATTACTGTCAGCAGTACGCCGCCT ACCCTACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTCTAC ATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGCAG GTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCTCAG TGAAGGTTTCCTGCAGGGCATCTGGATACACCTTCATGGAGCACTATAT GCACTGGGTGCGACAGGCCCCTGGACAAGGGCTTGAGTGGATGGGAGTA ATCGGGCCTAGTGGTGGTAAGACAAGCTACGCACAGAAGTTCCAGGGCA GAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGGAGCT GAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAGAG AATTGGCCAATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCT CAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGT GAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAG CCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTC TGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAG CCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGC CCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTG CCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGG GAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGG GTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCT GCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGA GAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCA CTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACC TAGG.

In further embodiments, the invention relates to Clone AJ-26545 CAR L×H AA sequence (SEQ ID NO: 312):

MALPVTALLL PLALLLHAAR PEIVMTQSPA TLSVSPGERA TLSCRASQSV SSNLAWYQQK PGQAPRLLIY GASTRATGIP ARFSGSGSGT EFTLTISSLQ SEDFAVYYCQ QYAAYPTFGG GTKVEIKRGS TSGSGKPGSG EGSTKGQVQL VQSGAEVKKP GASVKVSCRA SGYTFMEHYM HWVRQAPGQG LEWMGVIGPS GGKTSYAQKF QGRVTMTRDT STSTVYMELS SLRSEDTAVY YCARESWPMD VWGQGTTVTV SSAAALDNEK SNGTIIHVKG KHLCPSPLFP GPSKPFWVLV VVGGVLACYS LLVTVAFIIF WVRSKRSRLL HSDYMNMTPR RPGPTRKHYQ PYAPPRDFAA YRSRVKFSRS ADAPAYQQGQ NQLYNELNLG RREEYDVLDK RRGRDPEMGG KPRRKNPQEG LYNELQKDKM AEAYSEIGMK GERRRGKGHD GLYQGLSTAT KDTYDALHMQ ALPPR.

In further embodiments, the invention relates to Clone AJ-26554 HC DNA (SEQ ID NO: 313):

CAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCT CAGTGAAGGTTTCCTGCAAGGCATCTGGATACACCTTCACGGAGCACTA TATGCACTGGGTGCGACAGGCCCCTGGACAAAGGCTTGAGTGGATGGGA GTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGCACAGAAGTTCCAGG GCAGAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGGA GCTGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGA GAGAGTTGGCCAATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCT CCTCA.

In further embodiments, the invention relates to Clone AJ-26554 HC (SEQ ID NO: 314):

QVQLVQSGAE VKKPGASVKV SCKASGYTFT EHYMHWVRQA PGQRLEWMGV IGPSGGKTSY AQKFQGRVTM TRDTSTSTVY MELSSLRSED TAVYYCARES WPMDVWGOGT TVTVSS.

In further embodiments, the invention relates to HC CDR1 thereof: YTFTEHYMH (SEQ ID NO: 315). In further embodiments, the invention relates to HC CDR2 thereof: VIGPSGGKTSYAQKFQG (SEQ ID NO: 316). In further embodiments, the invention relates to HC CDR3 thereof: ARESWPMDV (SEQ ID NO: 317).

In further embodiments, the invention relates to Clone AJ-26554 LC DNA (SEQ ID NO: 318):

GAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGG AAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTT AGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTAT GGTGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTCAGTGGCAGTG GGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGA TTTTGCAGTTTATTACTGTCAGCAGTACGCCGCCTACCCTACTTTTGGC GGAGGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone AJ-26554 LC AA sequence (SEQ ID NO: 319):

EIVMTQSPAT LSVSPGERAT LSCRASQSVS SNLAWYQQKP GQAPRLLIYG ASTRATGIPA RFSGSGSGTE FTLTISSLQS EDFAVYYCQQ YAAYPTFGGG TKVEIKR.

In further embodiments, the invention relates to the LC CDR1 thereof: RASQSVSSNLA (SEQ ID NO: 320). In further embodiments, the invention relates to the LC CDR2 thereof: GASTRAT (SEQ ID NO: 321). In further embodiments, the invention relates to LC CDR3 thereof: QQYAAYPT (SEQ ID NO: 322).

In further embodiments, the invention relates to Clone AJ-26554 CAR DNA H×L (SEQ ID NO: 323):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAA GAAGCCTGGGGCCTCAGTGAAGGTTTCCTGCAAGGCATCTGGATACACC TTCACGGAGCACTATATGCACTGGGTGCGACAGGCCCCTGGACAAAGGC TTGAGTGGATGGGAGTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGC ACAGAAGTTCCAGGGCAGAGTCACCATGACCAGGGACACGTCCACGAGC ACAGTCTACATGGAGCTGAGCAGCCTGAGATCTGAGGACACGGCGGTGT ACTACTGCGCCAGAGAGAGTTGGCCAATGGACGTATGGGGCCAGGGAAC AACTGTCACCGTCTCCTCAGGGTCTACATCCGGCTCCGGGAAGCCCGGA AGTGGCGAAGGTAGTACAAAGGGGGAAATAGTGATGACGCAGTCTCCAG CCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGC CAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGC CAGGCTCCCAGGCTCCTCATCTATGGTGCATCCACCAGGGCCACTGGTA TCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCAC CATCAGCAGCCTGCAGTCTGAAGATTTTGCAGTTTATTACTGTCAGCAG TACGCCGCCTACCCTACTTTTGGCGGAGGGACCAAGGTTGAGATCAAAC GGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGT GAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAG CCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTC TGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAG CCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGC CCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTG CCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGG GAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGG GTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCT GCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGA GAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCA CTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACC TAGG.

In further embodiments, the invention relates to Clone AJ-26554 CAR H×L AA sequence (SEQ ID NO: 324):

MALPVTALLL PLALLLHAAR PQVQLVQSGA EVKKPGASVK VSCKASGYTF TEHYMHWVRQ APGQRLEWMG VIGPSGGKTS YAQKFQGRVT MTRDTSTSTV YMELSSLRSE DTAVYYCARE SWPMDVWGQG TTVTVSSGST SGSGKPGSGE GSTKGEIVMT QSPATLSVSP GERATLSCRA SQSVSSNLAW YQQKPGQAPR LLIYGASTRA TGIPARFSGS GSGTEFTLTI SSLQSEDFAV YYCQQYAAYP TFGGGTKVEI KRAAALDNEK SNGTIIHVKG KHLCPSPLFP GPSKPFWVLV VVGGVLACYS LLVTVAFIIF WVRSKRSRLL HSDYMNMTPR RPGPTRKHYQ PYAPPRDFAA YRSRVKFSRS ADAPAYQQGQ NQLYNELNLG RREEYDVLDK RRGRDPEMGG KPRRKNPQEG LYNELQKDKM AEAYSEIGMK GERRRGKGHD LYQGLSTAT KDTYDALHMQ ALPPR.

In further embodiments, the invention relates to Clone AJ-26554 CAR DNA L×H (SEQ ID NO: 325):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGGAAATAGTGATGACGCAGTCTCCAGCCACCCTGTC TGTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGT GTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCA GGCTCCTCATCTATGGTGCATCCACCAGGGCCACTGGTATCCCAGCCAG GTTCAGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGC CTGCAGTCTGAAGATTTTGCAGTTTATTACTGTCAGCAGTACGCCGCCT ACCCTACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTCTAC ATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGCAG GTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCTCAG TGAAGGTTTCCTGCAAGGCATCTGGATACACCTTCACGGAGCACTATAT GCACTGGGTGCGACAGGCCCCTGGACAAAGGCTTGAGTGGATGGGAGTA ATCGGGCCTAGTGGTGGTAAGACAAGCTACGCACAGAAGTTCCAGGGCA GAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGGAGCT GAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAGAG AGTTGGCCAATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCT CAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGT GAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAG CCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTC TGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAG CCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGC CCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTG CCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGG GAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGG GTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCT GCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGA GAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCA CTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACC TAGG.

In further embodiments, the invention relates to Clone AJ-26554 CAR L×H AA sequence (SEQ ID NO: 326):

MALPVTALLL PLALLLHAAR PEIVMTQSPA TLSVSPGERA TLSCRASQSV SSNLAWYQQK PGQAPRLLIY GASTRATGIP ARFSGSGSGT EFTLTISSLQ SEDFAVYYCQ QYAAYPTFGG GTKVEIKRGS TSGSGKPGSG EGSTKGQVQL VQSGAEVKKP GASVKVSCKA SGYTFTEHYM HWVRQAPGQR LEWMGVIGPS GGKTSYAQKF QGRVTMTRDT STSTVYMELS SLRSEDTAVY YCARESWPMD VWGQGTTVTV SSAAALDNEK SNGTIIHVKG KHLCPSPLFP GPSKPFWVLV VVGGVLACYS LLVTVAFIIF WVRSKRSRLL HSDYMNMTPR RPGPTRKHYQ PYAPPRDFAA YRSRVKFSRS ADAPAYQQGQ NQLYNELNLG RREEYDVLDK RRGRDPEMGG KPRRKNPQEG LYNELQKDKM AEAYSEIGMK GERRRGKGH DGLYQGLSTAT KDTYDALHMQ ALPPR.

In further embodiments, the invention relates to Clone NM-26562 HC DNA (SEQ ID NO: 327):

CAGGTGCAGCTGCAGGAGTCGGGCCCAGGACTGGTGAAGCCTTCACAGAC CCTGTCCCTCACCTGTACTGTCTCTGGTGGCTCCATCGGGAGTGGTGGTA GTTACTGGAGCTGGATCCGCCAGCACCCAGGGAAGGGCCTGGAGTGGATT GGGTTGATCTATTACGATGGGAGCACCTACTACAACCCGTCCCTCAAGAG TCGAGTTACCATATCAGTAGACACGTCTAAGAACCAGTTCTCCCTGAAGC TGAGTTCTGTGACCGCCGCAGACACGGCGGTGTACTACTGCGCCAGAGGC AGGGGATATGAGACTTCTTTAGCCTTCGATATCTGGGGTCAGGGTACAAT GGTCACCGTCTCCTCA.

In further embodiments, the invention relates to Clone NM-26562 HC AA sequence (SEQ ID NO: 328):

QVQLQESGPG LVKPSQTLSL TCTVSGGSIG SGGSYWSWIR QHPGKGLEWI GLIYYDGSTY YNPSLKSRVT ISVDTSKNQF SLKLSSVTAA DTAVYYCARG RGYETSLAFD IWGQGTMVTV SS.

In further embodiments, the invention relates to HC CDR1 thereof: GSIGSGGSYWS (SEQ ID NO: 329). In further embodiments, the invention relates to HC CDR2 thereof: LIYYDGSTYYNPSLKS (SEQ ID NO: 330). In further embodiments, the invention relates to HC CDR3 thereof: ARGRGYETSLAFDI (SEQ ID NO: 331).

In further embodiments, the invention relates to Clone NM-26562 LC DNA (SEQ ID NO: 332):

GAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGG AAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCTACTT AGCCTGGTACCAACAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTAT GATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTG GGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGA TTTTGCAGTTTATTACTGTCAGCAGAGACACGTCTGGCCTCCTACTTTT GGCGGAGGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone NM-26562 LC AA sequence (SEQ ID NO: 333):

EIVLTQSPAT LSLSPGERAT LSCRASQSVS SYLAWYQQKP GQAPRLLIYD ASNRATGIPA RFSGSGSGTD FTLTISSLEP EDFAVYYCQQ RHVWPPTFGG GTKVEIKR.

In further embodiments, the invention relates to LC CDR1 AA sequence thereof: RASQSVSSYLA (SEQ ID NO: 334) In further embodiments, the invention relates to LC CDR2 AA sequence thereof: DASNRAT (SEQ ID NO: 335). In further embodiments, the invention relates to LC CDR3 AA sequence thereof: QQRHVWPPT (SEQ ID NO: 336) (LC CDR3).

In further embodiments, the invention relates to Clone NM-26562 CAR DNA H×L (SEQ ID NO: 337):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGCAGGTGCAGCTGCAGGAGTCGGGCCCAGGACTGGT GAAGCCTTCACAGACCCTGTCCCTCACCTGTACTGTCTCTGGTGGCTCC ATCGGGAGTGGTGGTAGTTACTGGAGCTGGATCCGCCAGCACCCAGGGA AGGGCCTGGAGTGGATTGGGTTGATCTATTACGATGGGAGCACCTACTA CAACCCGTCCCTCAAGAGTCGAGTTACCATATCAGTAGACACGTCTAAG AACCAGTTCTCCCTGAAGCTGAGTTCTGTGACCGCCGCAGACACGGCGG TGTACTACTGCGCCAGAGGCAGGGGATATGAGACTTCTTTAGCCTTCGA TATCTGGGGTCAGGGTACAATGGTCACCGTCTCCTCAGGGTCTACATCC GGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATTG TGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGC CACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCTACTTAGCCTGG TACCAACAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTATGATGCAT CCAACAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGG GACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATTTTGCA GTTTATTACTGTCAGCAGAGACACGTCTGGCCTCCTACTTTTGGCGGAG GGACCAAGGTTGAGATCAAACGGGCCGCTGCCCTTGATAATGAAAAGTC AAACGGAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCC TTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTG GAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTT CTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAAT ATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACG CACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAG ATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAAC GAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCA GAGGACGGGACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCA GGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTAT TCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACG GTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCT CCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone NM-26562 CAR H×L (SEQ ID NO: 338):

MALPVTALLL PLALLLHAAR PQVQLQESGP GLVKPSQTLS LTCTVSGGSI GSGGSYWSWI RQHPGKGLEW IGLIYYDGST YYNPSLKSRV TISVDTSKNQ FSLKLSSVTA ADTAVYYCAR GRGYETSLAF DIWGQGTMVT VSSGSTSGSG KPGSGEGSTK GEIVLTQSPA TLSLSPGERA TLSCRASQSV SSYLAWYQQK PGQAPRLLIY DASNRATGIP ARFSGSGSGT DFTLTISSLE PEDFAVYYCQ QRHVWPPTFG GGTKVEIKRA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR.

In further embodiments, the invention relates to Clone NM-26562 CAR DNA L×H (SEQ ID NO: 339):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCAC GCCGCACGCCCGGAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTG TCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGC AGCTACTTAGCCTGGTACCAACAGAAACCTGGCCAGGCTCCCAGGCTCCTC ATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGC AGTGGGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAA GATTTTGCAGTTTATTACTGTCAGCAGAGACACGTCTGGCCTCCTACTTTT GGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTCTACATCCGGCTCCGGG AAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGCAGGTGCAGCTGCAGGAG TCGGGCCCAGGACTGGTGAAGCCTTCACAGACCCTGTCCCTCACCTGTACT GTCTCTGGTGGCTCCATCGGGAGTGGTGGTAGTTACTGGAGCTGGATCCGC CAGCACCCAGGGAAGGGCCTGGAGTGGATTGGGTTGATCTATTACGATGGG AGCACCTACTACAACCCGTCCCTCAAGAGTCGAGTTACCATATCAGTAGAC ACGTCTAAGAACCAGTTCTCCCTGAAGCTGAGTTCTGTGACCGCCGCAGAC ACGGCGGTGTACTACTGCGCCAGAGGCAGGGGATATGAGACTTCTTTAGCC TTCGATATCTGGGGTCAGGGTACAATGGTCACCGTCTCCTCAGCCGCTGCC CTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCAC CTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTG GTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCT TTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCATAGCGAT TACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCAG CCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTT TCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTAT AACGAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGC AGAGGACGGGACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAG GAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTATTCT GAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTG TACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATG CAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone NM-26562 CAR L×H (SEQ ID NO: 340):

MALPVTALLL PLALLLHAAR PEIVLTQSPA TLSLSPGERA TLSCRASQSV SSYLAWYQQK PGQAPRLLIY DASNRATGIP ARFSGSGSGT DFTLTISSLE PEDFAVYYCQ QRHVWPPTFG GGTKVEIKRG STSGSGKPGS GEGSTKGQVQ LQESGPGLVK PSQTLSLTCT VSGGSIGSGG SYWSWIRQHP GKGLEWIGLI YYDGSTYYNP SLKSRVTISV DTSKNQFSLK LSSVTAADTA VYYCARGRGY ETSLAFDIWG QGTMVTVSSA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR.

In further embodiments, the invention relates to Clone TS-26564 HC DNA sequence (SEQ ID NO: 341):

GAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGT CCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACCTTCAGTAGCTATAG CATGAACTGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTTTCA ACCATTAGTAGTAGTAGTAGTATCATATACTACGCAGACTCTGTGAAGG GCCGATTCACCATCTCCAGAGACAATGCCAAGAACTCACTGTATCTGCA AATGAACAGCCTGAGAGCTGAGGACACGGCGGTGTACTACTGCGCCAGA GGTTCTCAGGAGCACCTGATTTTCGATTATTGGGGACAGGGTACATTGG TCACCGTCTCCTCA.

In further embodiments, the invention relates to Clone TS-26564 HC AA sequence (SEQ ID NO: 342):

EVQLVESGGG LVQPGGSLRL SCAASGFTFS SYSMNWVRQA PGKGLEWVST ISSSSSIIYY ADSVKGRFTI SRDNAKNSLY LQMNSLRAED TAVYYCARGS QEHLIFDYWG QGTLVTVSS.

In further embodiments, the invention relates to HC CDR1 AA sequence thereof: FTFSSYSMN (SEQ ID NO: 343). In further embodiments, the invention relates to HC CDR2 AA sequence thereof: TISSSSSIIYYADSVKG (SEQ ID NO: 344). In further embodiments, the invention relates to HC CDR3 AA sequence thereof: ARGSQEHLIFDY (SEQ ID NO: 345).

In further embodiments, the invention relates to Clone TS-26564 LC DNA (SEQ ID NO: 346):

GAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGG AAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGGTACTT AGCCTGGTACCAACAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTAT GATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTG GGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGA TTTTGCAGTTTATTACTGTCAGCAGAGATTCTACTACCCTTGGACTTTT GGCGGAGGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone TS-26564 LC AA sequence (SEQ ID NO: 347):

EIVLTQSPAT LSLSPGERAT LSCRASQSVS RYLAWYQQKP GQAPRLLIYD ASNRATGIPA RFSGSGSGTD FTLTISSLEP EDFAVYYCQQ RFYYPWTFGG GTKVEIKR.

In further embodiments, the invention relates to LC CDR1 AA sequence thereof: RASQSVSRYLA (SEQ ID NO: 348). In further embodiments, the invention relates to LC CDR2 AA sequence thereof: DASNRAT (SEQ ID NO: 349). In further embodiments, the invention relates to LC CDR3 AA sequence thereof: QQRFYYPWT (SEQ ID NO: 350).

In further embodiments, the invention relates to Clone TS-26564 CAR DNA H×L (SEQ ID NO: 351):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGGAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTGGT ACAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACC TTCAGTAGCTATAGCATGAACTGGGTCCGCCAGGCTCCAGGGAAGGGGC TGGAGTGGGTTTCAACCATTAGTAGTAGTAGTAGTATCATATACTACGC AGACTCTGTGAAGGGCCGATTCACCATCTCCAGAGACAATGCCAAGAAC TCACTGTATCTGCAAATGAACAGCCTGAGAGCTGAGGACACGGCGGTGT ACTACTGCGCCAGAGGTTCTCAGGAGCACCTGATTTTCGATTATTGGGG ACAGGGTACATTGGTCACCGTCTCCTCAGGGTCTACATCCGGCTCCGGG AAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATTGTGTTGACAC AGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTC CTGCAGGGCCAGTCAGAGTGTTAGCAGGTACTTAGCCTGGTACCAACAG AAACCTGGCCAGGCTCCCAGGCTCCTCATCTATGATGCATCCAACAGGG CCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGACTT CACTCTCACCATCAGCAGCCTAGAGCCTGAAGATTTTGCAGTTTATTAC TGTCAGCAGAGATTCTACTACCCTTGGACTTTTGGCGGAGGGACCAAGG TTGAGATCAAACGGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAAC AATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCT GGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCG CTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAG ATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCA CGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTA GAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGA TGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAAC CTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGG ACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCT CTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATA GGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACC AGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCA AGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone TS-26564 CAR H×L AA sequence (SEQ ID NO: 352):

MALPVTALLL PLALLLHAAR PEVQLVESGG GLVQPGGSLR LSCAASGFTF SSYSMNWVRQ APGKGLEWVS TISSSSSIIY YADSVKGRFT ISRDNAKNSL YLQMNSLRAE DTAVYYCARG SQEHLIFDYW GQGTLVTVSS GSTSGSGKPG SGEGSTKGEI VLTQSPATLS LSPGERATLS CRASQSVSRY LAWYQQKPGQ APRLLIYDAS NRATGIPARF SGSGSGTDFT LTISSLEPED FAVYYCQQRF YYPWTFGGGT KVEIKRAAAL DNEKSNGTII HVKGKHLCPS PLFPGPSKPF WVLVVVGGVL ACYSLLVTVA FIIFWVRSKR SRLLHSDYMN MTPRRPGPTR KHYQPYAPPR DFAAYRSRVK FSRSADAPAY QQGQNQLYNE LNLGRREEYD VLDKRRGRDP EMGGKPRRKN PQEGLYNELQ KDKMAEAYSE IGMKGERRRG KGHDGLYQGL STATKDTYDA LHMQALPPR.

In further embodiments, the invention relates to Clone TS-26564 CAR DNA L×H (SEQ ID NO: 353):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGC ACGCCGCACGCCCGGAAATTGTGTTGACACAGTCTCCAGCCACCCTGTC TTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGT GTTAGCAGGTACTTAGCCTGGTACCAACAGAAACCTGGCCAGGCTCCCA GGCTCCTCATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAG GTTCAGTGGCAGTGGGTCTGGGACAGACTTCACTCTCACCATCAGCAGC CTAGAGCCTGAAGATTTTGCAGTTTATTACTGTCAGCAGAGATTCTACT ACCCTTGGACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTC TACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGG GAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGT CCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACCTTCAGTAGCTATAG CATGAACTGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTTTCA ACCATTAGTAGTAGTAGTAGTATCATATACTACGCAGACTCTGTGAAGG GCCGATTCACCATCTCCAGAGACAATGCCAAGAACTCACTGTATCTGCA AATGAACAGCCTGAGAGCTGAGGACACGGCGGTGTACTACTGCGCCAGA GGTTCTCAGGAGCACCTGATTTTCGATTATTGGGGACAGGGTACATTGG TCACCGTCTCCTCAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAAC AATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCT GGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCG CTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAG ATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCA CGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTA GAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGA TGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAAC CTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGG ACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCT CTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATA GGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACC AGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCA AGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone TS-26564 CAR L×H AA sequence (SEQ ID NO: 354):

MALPVTALLL PLALLLHAAR PEIVLTQSPA TLSLSPGERA TLSCRASQSV SRYLAWYQQK PGQAPRLLIY DASNRATGIP ARFSGSGSGT DFTLTISSLE PEDFAVYYCQ QRFYYPWTFG GGTKVEIKRG STSGSGKPGS GEGSTKGEVQ LVESGGGLVQ PGGSLRLSCA ASGFTFSSYS MNWVRQAPGK GLEWVSTISS SSSIIYYADS VKGRFTISRD NAKNSLYLQM NSLRAEDTAV YYCARGSQEH LIFDYWGQGT LVTVSSAAAL DNEKSNGTII HVKGKHLCPS PLFPGPSKPF WVLVVVGGVL ACYSLLVTVA FIIFWVRSKR SRLLHSDYMN MTPRRPGPTR KHYQPYAPPR DFAAYRSRVK FSRSADAPAY QQGQNQLYNE LNLGRREEYD VLDKRRGRDP EMGGKPRRKN PQEGLYNELQ KDKMAEAYSE IGMKGERRRG KGHDGLYQGL STATKDTYDA LHMQALPPR.

In further embodiments, the invention relates to Clone RY-26568 HC DNA (SEQ ID NO: 355):

CAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGT CCCTGAGACTCTCCTGTGCAGCGTCTGGATTCACCTTCGGGAGCTATGG CATGCACTGGGTCCGCCAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCA GTTATACATTATGATGGAAGTGTTGAATACTATGCAGACTCCGTGAAGG GCCGATTCACCATCTCCAGAGACAATTCCAAGGACACGCTGTATCTGCA AATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCCAGA ACTGACTTCTGGAGCGGATCCCCTCCAAGCTTAGATTACTGGGGACAGG GTACATTGGTCACCGTCTCCTCA.

In further embodiments, the invention relates to Clone RY-26568 HC AA sequence (SEQ ID NO: 356):

QVQLVESGGG VVQPGRSLRL SCAASGFTFG SYGMHWVRQA PGKGLEWVAV IHYDGSVEYY ADSVKGRFTI SRDNSKDTLY LQMNSLRAED TAVYYCARTD FWSGSPPSLD YWGQGTLVTV SS.

In further embodiments, the invention relates to HC CDR1 thereof: FTFGSYGMH (SEQ ID NO: 357). In further embodiments, the invention relates to HC CDR2 thereof: VIHYDGSVEYYADSVKG (SEQ ID NO: 358). In further embodiments, the invention relates to HC CDR3 thereof: ARTDFWSGSPPSLDY (SEQ ID NO: 359).

In further embodiments, the invention relates to Clone RY-26568 LC DNA (SEQ ID NO: 360):

GACATCCAGTTGACCCAGTCTCCATCTTCCGTGTCTGCATCTGTAGGAGA CAGAGTCACCATCACTTGTCGGGCGAGTCGGGGTATTAGCAGCTGGTTAG CCTGGTATCAGCAGAAACCAGGGAAAGCCCCTAAGCTCCTGATCTATGGT GCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTTCAGCGGCAGTGGATC TGGGACAGATTTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTG CAACTTATTACTGTCAGCAGATATACACCTTCCCTTTCACTTTTGGCGGA GGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone RY-26568 LC AA sequence (SEQ ID NO: 361):

DIQLTQSPSS VSASVGDRVT ITCRASRGIS SWLAWYQQKP GKAPKLLIYG ASSLQSGVPS RFSGSGSGTD FTLTISSLQP EDFATYYCQQ IYTFPFTFGG GTKVEIKR.

In further embodiments, the invention relates to LC CDR1 AA sequence thereof: RASRGISSWLA (SEQ ID NO: 362). In further embodiments, the invention relates to LC CDR2 AA sequence thereof: GASSLQS (SEQ ID NO: 363). In further embodiments, the invention relates to LC CDR3 AA sequence thereof: QQIYTFPFT (SEQ ID NO: 364) (LC CDR3).

In further embodiments, the invention relates to Clone RY-26568 CAR DNA H×L (SEQ ID NO: 365):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCA CGCCGCACGCCCGCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCC AGCCTGGGAGGTCCCTGAGACTCTCCTGTGCAGCGTCTGGATTCACCTTC GGGAGCTATGGCATGCACTGGGTCCGCCAGGCTCCAGGCAAGGGGCTGGA GTGGGTGGCAGTTATACATTATGATGGAAGTGTTGAATACTATGCAGACT CCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGGACACGCTG TATCTGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTG CGCCAGAACTGACTTCTGGAGCGGATCCCCTCCAAGCTTAGATTACTGGG GACAGGGTACATTGGTCACCGTCTCCTCAGGGTCTACATCCGGCTCCGGG AAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGACATCCAGTTGACCCA GTCTCCATCTTCCGTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTT GTCGGGCGAGTCGGGGTATTAGCAGCTGGTTAGCCTGGTATCAGCAGAAA CCAGGGAAAGCCCCTAAGCTCCTGATCTATGGTGCATCCAGTTTGCAAAG TGGGGTCCCATCAAGGTTCAGCGGCAGTGGATCTGGGACAGATTTCACTC TCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGTCAG CAGATATACACCTTCCCTTTCACTTTTGGCGGAGGGACCAAGGTTGAGAT CAAACGGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTC ACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCC AAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTC TCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAA GCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGC CCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGC CTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATC AGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGAA GAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGG CAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGA AGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGG AGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTAC GAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone RY-26568 CAR H×L AA sequence (SEQ ID NO: 366):

MALPVTALLL PLALLLHAAR PQVQLVESGG GVVQPGRSLR LSCAASGFTF GSYGMHWVRQ APGKGLEWVA VIHYDGSVEY YADSVKGRFT ISRDNSKDTL YLQMNSLRAE DTAVYYCART DFWSGSPPSL DYWGQGTLVT VSSGSTSGSG KPGSGEGSTK GDIQLTQSPS SVSASVGDRV TITCRASRGI SSWLAWYQQK PGKAPKLLIY GASSLQSGVP SRFSGSGSGT DFTLTISSLQ PEDFATYYCQ QIYTFPFTFG GGTKVEIKRA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR.

In further embodiments, the invention relates to Clone RY-26568 CAR DNA L×H (SEQ ID NO: 367):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCA CGCCGCACGCCCGGACATCCAGTTGACCCAGTCTCCATCTTCCGTGTCTG CATCTGTAGGAGACAGAGTCACCATCACTTGTCGGGCGAGTCGGGGTATT AGCAGCTGGTTAGCCTGGTATCAGCAGAAACCAGGGAAAGCCCCTAAGCT CCTGATCTATGGTGCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTTCA GCGGCAGTGGATCTGGGACAGATTTCACTCTCACCATCAGCAGCCTGCAG CCTGAAGATTTTGCAACTTATTACTGTCAGCAGATATACACCTTCCCTTT CACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTCTACATCCG GCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGCAGGTGCAG CTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACT CTCCTGTGCAGCGTCTGGATTCACCTTCGGGAGCTATGGCATGCACTGGG TCCGCCAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTTATACATTAT GATGGAAGTGTTGAATACTATGCAGACTCCGTGAAGGGCCGATTCACCAT CTCCAGAGACAATTCCAAGGACACGCTGTATCTGCAAATGAACAGCCTGA GAGCCGAGGACACGGCGGTGTACTACTGCGCCAGAACTGACTTCTGGAGC GGATCCCCTCCAAGCTTAGATTACTGGGGACAGGGTACATTGGTCACCGT CTCCTCAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTC ACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCC AAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTC TCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAA GCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGC CCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGC CTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATC AGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGAA GAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGG CAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGA AGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGG AGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTAC GAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone RY-26568 CAR L×H AA sequence (SEQ ID NO: 368):

MALPVTALLL PLALLLHAAR PDIQLTQSPS SVSASVGDRV TITCRASRGI SSWLAWYQQK PGKAPKLLIY GASSLQSGVP SRFSGSGSGT DFTLTISSLQ PEDFATYYCQ QIYTFPFTFG GGTKVEIKRG STSGSGKPGS GEGSTKGQVQ LVESGGGVVQ PGRSLRLSCA ASGFTFGSYG MHWVRQAPGK GLEWVAVIHY DGSVEYYADS VKGRFTISRD NSKDTLYLQM NSLRAEDTAV YYCARTDFWS GSPPSLDYWG QGTLVTVSSA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR.

In further embodiments, the invention relates to Clone PP-26575 HC DNA (SEQ ID NO: 369):

CAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGTCCTC GGTGAAGGTCTCCTGCAAGGCTTCTGGAGGCACCCTCAGCAGCCTGGCTA TCAGCTGGGTGCGACAGGCCCCTGGACAAGGGCTTGAGTGGATGGGAGGG GTCATCCCTATCTTGGGTCGGGCAAACTACGCACAGAAGTTCCAGGGCAG AGTCACGATTACCGCGGACGAGTCCACGAGCACAGCCTACATGGAGCTGA GCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAACTCCT GAATACTCCTCCAGCATATGGCACTATTACTACGGCATGGACGTATGGGG CCAGGGAACAACTGTCACCGTCTCCTCA.

In further embodiments, the invention relates to Clone PP-26575 HC AA sequence (SEQ ID NO: 370):

QVQLVQSGAE VKKPGSSVKV SCKASGGTLS SLAISWVRQA PGQGLEWMGG VIPILGRANY AQKFQGRVTI TADESTSTAY MELSSLRSED TAVYYCARTP EYSSSIWHYY YGMDVWGQGT TVTVSS.

In further embodiments, the invention relates to HC CDR1 AA sequence thereof: GILSSLAIS (SEQ ID NO: 371). In further embodiments, the invention relates to HC CDR2 AA sequence thereof: GVIPILGRANYAQKFQG (SEQ ID NO: 372). In further embodiments, the invention relates to HC CDR3 thereof: ARTPEYSSSIWHYYYGMDV (SEQ ID NO: 373).

In further embodiments, the invention relates to Clone PP-26575 LC DNA (SEQ ID NO: 374):

GACATCGTGATGACCCAGTCTCCAGACTCCCTGGCTGTGTCTCTGGGCGA GAGGGCCACCATCAACTGCAAGTCCAGCCAGAGTGTTTTATACAGCTCCA ACAATAAGAACTACTTAGCTTGGTACCAGCAGAAACCAGGACAGCCTCCT AAGCTGCTCATTTACTGGGCATCTACCCGGGAATCCGGGGTCCCTGACCG ATTCAGTGGCAGCGGGTCTGGGACAGATTTCACTCTCACCATCAGCAGCC TGCAGGCTGAAGATGTGGCAGTTTATTACTGTCAGCAGTTCGCCCACACT CCTTTCACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone PP-26575 LC AA sequence (SEQ ID NO: 375):

DIVMTQSPDS LAVSLGERAT INCKSSQSVL YSSNNKNYLA WYQQKPGQPP KLLIYWASTR ESGVPDRFSG SGSGTDFTLT ISSLQAEDVA VYYCQQFAHT PFTFGGGTKV EIKR.

In further embodiments, the invention relates to LC CDR 1 AA sequence thereof: KSSQSVLYSSNNKNYLA (SEQ ID NO: 376). In further embodiments, the invention relates to LC CDR2 AA sequence thereof: WASTRES (SEQ ID NO: 377). In further embodiments, the invention relates to LC CDR3 AA sequence thereof: QQFAHTPFT (SEQ ID NO: 378).

In further embodiments, the invention relates to Clone PP-26575 CAR DNA H×L (SEQ ID NO: 379):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCA CGCCGCACGCCCGCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGA AGCCTGGGTCCTCGGTGAAGGTCTCCTGCAAGGCTTCTGGAGGCACCCTC AGCAGCCTGGCTATCAGCTGGGTGCGACAGGCCCCTGGACAAGGGCTTGA GTGGATGGGAGGGGTCATCCCTATCTTGGGTCGGGCAAACTACGCACAGA AGTTCCAGGGCAGAGTCACGATTACCGCGGACGAGTCCACGAGCACAGCC TACATGGAGCTGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTG CGCCAGAACTCCTGAATACTCCTCCAGCATATGGCACTATTACTACGGCA TGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCAGGGTCTACA TCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGACAT CGTGATGACCCAGTCTCCAGACTCCCTGGCTGTGTCTCTGGGCGAGAGGG CCACCATCAACTGCAAGTCCAGCCAGAGTGTTTTATACAGCTCCAACAAT AAGAACTACTTAGCTTGGTACCAGCAGAAACCAGGACAGCCTCCTAAGCT GCTCATTTACTGGGCATCTACCCGGGAATCCGGGGTCCCTGACCGATTCA GTGGCAGCGGGTCTGGGACAGATTTCACTCTCACCATCAGCAGCCTGCAG GCTGAAGATGTGGCAGTTTATTACTGTCAGCAGTTCGCCCACACTCCTTT CACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGCCGCTGCCCTTG ATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTC TGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGT CGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTT TTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCATAGCGAT TACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCA GCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGT TTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTG TATAACGAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAA GCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACC CCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCC TATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGA CGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTC TCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone PP-26575 CAR H×L AA sequence (SEO TD NO: 3801:

MALPVTALLL PLALLLHAAR PQVQLVQSGA EVKKPGSSVK VSCKASGGTL SSLAISWVRQ APGQGLEWMG GVIPILGRAN YAQKFQGRVT ITADESTSTA YMELSSLRSE DTAVYYCART PEYSSSIWHY YYGMDVWGOG TTVTVSSGST SGSGKPGSGE GSTKGDIVMT QSPDSLAVSL GERATINCKS SQSVLYSSNN KNYLAWYQQK PGQPPKLLIY WASTRESGVP DRFSGSGSGT DFTLTISSLQ AEDVAVYYCQ QFAHTPFTFG GGTKVEIKRA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR.

In further embodiments, the invention relates to Clone PP-26575 CAR DNA L×H (SEQ ID NO: 381):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCA CGCCGCACGCCCGGACATCGTGATGACCCAGTCTCCAGACTCCCTGGCTG TGTCTCTGGGCGAGAGGGCCACCATCAACTGCAAGTCCAGCCAGAGTGTT TTATACAGCTCCAACAATAAGAACTACTTAGCTTGGTACCAGCAGAAACC AGGACAGCCTCCTAAGCTGCTCATTTACTGGGCATCTACCCGGGAATCCG GGGTCCCTGACCGATTCAGTGGCAGCGGGTCTGGGACAGATTTCACTCTC ACCATCAGCAGCCTGCAGGCTGAAGATGTGGCAGTTTATTACTGTCAGCA GTTCGCCCACACTCCTTTCACTTTTGGCGGAGGGACCAAGGTTGAGATCA AACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGT ACAAAGGGGCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCC TGGGTCCTCGGTGAAGGTCTCCTGCAAGGCTTCTGGAGGCACCCTCAGCA GCCTGGCTATCAGCTGGGTGCGACAGGCCCCTGGACAAGGGCTTGAGTGG ATGGGAGGGGTCATCCCTATCTTGGGTCGGGCAAACTACGCACAGAAGTT CCAGGGCAGAGTCACGATTACCGCGGACGAGTCCACGAGCACAGCCTACA TGGAGCTGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCC AGAACTCCTGAATACTCCTCCAGCATATGGCACTATTACTACGGCATGGA CGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCAGCCGCTGCCCTTG ATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTC TGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGT CGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTT TTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCATAGCGAT TACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCA GCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGT TTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTG TATAACGAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAA GCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACC CCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCC TATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGA CGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTC TCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone PP-26575 CAR L×H AA sequence (SEQ ID NO: 382):

MALPVTALLL PLALLLHAAR PDIVMTQSPD SLAVSLGERA TINCKSSQSV LYSSNNKNYL AWYQQKPGQP PKLLIYWAST RESGVPDRFS GSGSGTDFTL TISSLQAEDV AVYYCQQFAH TPFTFGGGTK VEIKRGSTSG SGKPGSGEGS TKGQVQLVQS GAEVKKPGSS VKVSCKASGG TLSSLAISWV RQAPGQGLEW MGGVIPILGR ANYAQKFQGR VTITADESTS TAYMELSSLR SEDTAVYYCA RTPEYSSSIW HYYYGMDVWG QGTTVTVSSA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR.

In further embodiments, the invention relates to Clone RD-26576 HC DNA (SEQ ID NO: 383):

CAGGTGCGGCTGGTGGAGTCTGGGGGGGGCGTGGTCCAGCCTGGGAGGTC CCTGAGACTCTCCTGTGCAGCGTCTGGATTCACCTTCAGTAGCTATGGCA TACACTGGGTCCGCCAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTT ATAGGGTATGATGGACAGGAGAAATACTATGCAGACTCCGTGAAGGGCCG ATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAATGA ACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCG TTGCAGGAGCCGCCATACGCTTTTGGGATGGACGTATGGGGCCAGGGAAC AACTGTCACCGTCTCCTCA.

In further embodiments, the invention relates to Clone RD-26576 HC AA sequence (SEQ ID NO: 384):

QVRLVESGGG VVQPGRSLRL SCAASGFTFS SYGIHWVRQA PGKGLEWVAV IGYDGQEKYY ADSVKGRFTI SRDNSKNTLY LQMNSLRAED TAVYYCVKGP LQEPPYAFGM DVWGQGTTVT VSS.

In further embodiments, the invention relates to HC CDR1 AA sequence thereof: FTFSSYGIH (SEQ ID NO: 385). In further embodiments, the invention relates to HC CDR2 AA sequence thereof: VIGYDGQEKYYADSVKG (SEQ ID NO: 386). In further embodiments, the invention relates to the HC CDR3 AA sequence thereof: VKGPLQEPPYAFGMDV (SEQ ID NO: 387).

In further embodiments, the invention relates to Clone RD-26576 LC DNA (SEQ ID NO: 388):

GAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGA AAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAG CCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTATAGC GCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTCAGTGGCAGTGGGTC TGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATTTTG CAGTTTATTACTGTCAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGA GGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone RD-26576 LC AA sequence (SEQ ID NO: 389):

EIVMTQSPAT LSVSPGERAT LSCRASQSVS SNLAWYQQKP GQAPRLLIYS ASTRATGIPA RFSGSGSGTE FTLTISSLQS EDFAVYYCQQ HHVWPLTFGG GTKVEIKR.

In further embodiments, the invention relates to LC CDR1 AA sequence thereof: RASQSVSSNLA (SEQ ID NO: 390). In further embodiments, the invention relates to LC CDR2 AA sequence thereof: SASTRAT (SEQ ID NO: 391). In further embodiments, the invention relates to LC CDR3 AA sequence thereof: QQHHVWPLT (SEQ ID NO: 392).

In further embodiments, the invention relates to Clone RD-26576 CAR DNA H×L (SEQ ID NO: 393):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCA CGCCGCACGCCCGCAGGTGCGGCTGGTGGAGTCTGGGGGGGGCGTGGTCC AGCCTGGGAGGTCCCTGAGACTCTCCTGTGCAGCGTCTGGATTCACCTTC AGTAGCTATGGCATACACTGGGTCCGCCAGGCTCCAGGCAAGGGGCTGGA GTGGGTGGCAGTTATAGGGTATGATGGACAGGAGAAATACTATGCAGACT CCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTG TATCTGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTG CGTCAAGGGGCCGTTGCAGGAGCCGCCATACGCTTTTGGGATGGACGTAT GGGGCCAGGGAACAACTGTCACCGTCTCCTCAGGGTCTACATCCGGCTCC GGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATAGTGATGAC GCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCTCT CCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAG AAACCTGGCCAGGCTCCCAGGCTCCTCATCTATAGCGCATCCACCAGGGC CACTGGTATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGAGTTCA CTCTCACCATCAGCAGCCTGCAGTCTGAAGATTTTGCAGTTTATTACTGT CAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGAGGGACCAAGGTTGA GATCAAACGGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCA TTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCA TCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTA CTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAA GAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCT GGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGC TGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGT ATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGG GAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGG TGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGC AGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAG CGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGC TACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone RD-26576 CAR H×L AA sequence (SEQ ID NO: 394):

MALPVTALLL PLALLLHAAR PQVRLVESGG GVVQPGRSLR LSCAASGFTF SSYGIHWVRQ APGKGLEWVA VIGYDGQEKY YADSVKGRFT ISRDNSKNTL YLQMNSLRAE DTAVYYCVKG PLQEPPYAFG MDVWGQGTTV TVSSGSTSGS GKPGSGEGST KGEIVMTQSP ATLSVSPGER ATLSCRASQS VSSNLAWYQQ KPGQAPRLLI YSASTRATGI PARFSGSGSG TEFTLTISSL QSEDFAVYYC QQHHVWPLTF GGGTKVEIKR AAALDNEKSN GTIIHVKGKH LCPSPLFPGP SKPFWVLVVV GGVLACYSLL VTVAFIIFWV RSKRSRLLHS DYMNMTPRRP GPTRKHYQPY APPRDFAAYR SRVKFSRSAD APAYQQGQNQ LYNELNLGRR EEYDVLDKRR GRDPEMGGKP RRKNPQEGLY NELQKDKMAE AYSEIGMKGE RRRGKGHDGL YQGLSTATKD TYDALHMQAL PPR.

In further embodiments, the invention relates to Clone RD-26576 CAR DNA L×H (SEQ ID NO: 395):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCA CGCCGCACGCCCGGAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTG TGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTT AGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCT CCTCATCTATAGCGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTCA GTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAG TCTGAAGATTTTGCAGTTTATTACTGTCAGCAGCACCACGTCTGGCCTCT CACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTCTACATCCG GCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGCAGGTGCGG CTGGTGGAGTCTGGGGGGGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACT TCCTGTGCAGCGTCTGGATTCACCTTCAGTAGCTATGGCATACACTGGGT CCGCCAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTTATAGGGTATG ATGGACAGGAGAAATACTATGCAGACTCCGTGAAGGGCCGATTCACCATC TCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAATGAACAGCCTGAG AGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCGTTGCAGGAGC CGCCATACGCTTTTGGGATGGACGTATGGGGCCAGGGAACAACTGTCACC GTCTCCTCAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCAT TCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCAT CCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTAC TCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAG AAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTG GCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCT GCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGG AAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGT GGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCA GAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGC GGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCT ACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone RD-26576 CAR L×H AA sequence (SEQ ID NO: 396):

MALPVTALLL PLALLLHAAR PEIVMTQSPA TLSVSPGERA TLSCRASQSV SSNLAWYQQK PGQAPRLLIY SASTRATGIP ARFSGSGSGT EFTLTISSLQ SEDFAVYYCQ QHHVWPLTFG GGTKVEIKRG STSGSGKPGS GEGSTKGQVR LVESGGGVVQ PGRSLRLSCA ASGFTFSSYG IHWVRQAPGK GLEWVAVIGY DGQEKYYADS VKGRFTISRD NSKNTLYLQM NSLRAEDTAV YYCVKGPLQE PPYAFGMDVW GQGTTVTVSS AAALDNEKSN GTIIHVKGKH LCPSPLFPGP SKPFWVLVVV GGVLACYSLL VTVAFIIFWV RSKRSRLLHS DYMNMTPRRP GPTRKHYQPY APPRDFAAYR SRVKFSRSAD APAYQQGQNQ LYNELNLGRR EEYDVLDKRR GRDPEMGGKP RRKNPQEGLY NELQKDKMAE AYSEIGMKGE RRRGKGHDGL YQGLSTATKD TYDALHMQAL PPR.

In further embodiments, the invention relates to Clone RD-26578 HC DNA (SEQ ID NO: 397):

CAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTC CCTGAGACTCTCCTGTGCAGCGTCTGGATTCACCTTCAGTAGCCGTGGCA TGCACTGGGTCCGCCAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTT ATAGGGTATGATGGACAGGAGAAATACTATGCAGACTCCGTGAAGGGCCG ATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAATGA ACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCG TTGCAGGAGCCGCCATACGATTATGGAATGGACGTATGGGGCCAGGGAAC AACTGTCACCGTCTCCTCA.

In further embodiments, the invention relates to Clone RD-26578 HC AA sequence (SEQ ID NO: 398):

QVQLVESGGG VVQPGRSLRL SCAASGFTFS SRGMHWVRQA PGKGLEWVAV IGYDGQEKYY ADSVKGRFTI SRDNSKNTLY LQMNSLRAED TAVYYCVKGP LQEPPYDYGM DVWGQGTTVT VSS.

In further embodiments, the invention relates to HC CDR1 AA sequence thereof: FTFSSRGMH (SEQ ID NO: 399). In further embodiments, the invention relates to HC CDR2 AA sequence thereof: VIGYDGQEKYYADSVKG (SEQ ID NO: 400). In further embodiments, the invention relates to HC CDR3 thereof: VKGPLQEPPYDYGMDV (SEQ ID NO: 401).

In further embodiments, the invention relates to Clone RD-26578 LC DNA (SEQ ID NO: 402):

GAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGA AAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAG CCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTATAGC GCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTCAGTGGCAGTGGGTC TGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATTTTG CAGTTTATTACTGTCAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGA GGGACCAAGGTTGAGATCAAACGG.

In further embodiments, the invention relates to Clone RD-26578 LC AA sequence (SEQ ID NO: 403):

EIVMTQSPAT LSVSPGERAT LSCRASQSVS SNLAWYQQKP GQAPRLLIYS ASTRATGIPA RFSGSGSGTE FTLTISSLQS EDFAVYYCQQ HHVWPLTFGG GTKVEIKR.

In further embodiments, the invention relates to LC CDR1 AA sequence: RASQSVSSNLA (SEQ ID NO: 404). In further embodiments, the invention relates to LC CDR2 AA sequence thereof: SASTRAT (SEQ ID NO: 405). In further embodiments, the invention relates to LC CDR3 AA sequence thereof: QQHHVWPLT (SEQ ID NO: 406).

In further embodiments, the invention relates to Clone RD-26578 CAR DNA H×L (SEQ ID NO: 407):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCA CGCCGCACGCCCGCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCC AGCCTGGGAGGTCCCTGAGACTCTCCTGTGCAGCGTCTGGATTCACCTTC AGTAGCCGTGGCATGCACTGGGTCCGCCAGGCTCCAGGCAAGGGGCTGGA GTGGGTGGCAGTTATAGGGTATGATGGACAGGAGAAATACTATGCAGACT CCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTG TATCTGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTG CGTCAAGGGGCCGTTGCAGGAGCCGCCATACGATTATGGAATGGACGTAT GGGGCCAGGGAACAACTGTCACCGTCTCCTCAGGGTCTACATCCGGCTCC GGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATAGTGATGAC GCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCTCT CCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAG AAACCTGGCCAGGCTCCCAGGCTCCTCATCTATAGCGCATCCACCAGGGC CACTGGTATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGAGTTCA CTCTCACCATCAGCAGCCTGCAGTCTGAAGATTTTGCAGTTTATTACTGT CAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGAGGGACCAAGGTTGA GATCAAACGGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCA TTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCA TCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTA CTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAA GAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCT GGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGC TGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGT ATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGG GAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGG TGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGC AGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAG CGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGC TACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone RD-26578 CAR H×L AA sequence (SEQ ID NO: 408):

MALPVTALLL PLALLLHAAR PQVQLVESGG GVVQPGRSLR LSCAASGFTF SSRGMHWVRQ APGKGLEWVA VIGYDGQEKY YADSVKGRFT ISRDNSKNTL YLQMNSLRAE DTAVYYCVKG PLQEPPYDYG MDVWGQGTTV TVSSGSTSGS GKPGSGEGST KGEIVMTQSP ATLSVSPGER ATLSCRASQS VSSNLAWYQQ KPGQAPRLLI YSASTRATGI PARFSGSGSG TEFTLTISSL QSEDFAVYYC QQHHVWPLTF GGGTKVEIKR AAALDNEKSN GTIIHVKGKH LCPSPLFPGP SKPFWVLVVV GGVLACYSLL VTVAFIIFWV RSKRSRLLHS DYMNMTPRRP GPTRKHYQPY APPRDFAAYR SRVKFSRSAD APAYQQGQNQ LYNELNLGRR EEYDVLDKRR GRDPEMGGKP RRKNPQEGLY NELQKDKMAE AYSEIGMKGE RRRGKGHDGL YQGLSTATKD TYDALHMQAL PPR.

In further embodiments, the invention relates to Clone RD-26578 CAR DNA L×H (SEQ ID NO: 409):

ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCA CGCCGCACGCCCGGAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTG TGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTT AGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCT CCTCATCTATAGCGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTCA GTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAG TCTGAAGATTTTGCAGTTTATTACTGTCAGCAGCACCACGTCTGGCCTCT CACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTCTACATCCG GCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGCAGGTGCAG CTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACT CTCCTGTGCAGCGTCTGGATTCACCTTCAGTAGCCGTGGCATGCACTGGG TCCGCCAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTTATAGGGTAT GATGGACAGGAGAAATACTATGCAGACTCCGTGAAGGGCCGATTCACCAT CTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAATGAACAGCCTGA GAGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCGTTGCAGGAG CCGCCATACGATTATGGAATGGACGTATGGGGCCAGGGAACAACTGTCAC CGTCTCCTCAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCA TTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCA TCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTA CTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAA GAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCT GGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGC TGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGT ATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGG GAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGG TGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGC AGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAG CGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGC TACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG.

In further embodiments, the invention relates to Clone RD-26578 CAR L×H AA sequence (SEQ ID NO: 410):

MALPVTALLL PLALLLHAAR PEIVMTQSPA TLSVSPGERA TLSCRASQSV SSNLAWYQQK PGQAPRLLIY SASTRATGIP ARFSGSGSGT EFTLTISSLQ SEDFAVYYCQ QHHVWPLTFG GGTKVEIKRG STSGSGKPGS GEGSTKGQVQ LVESGGGVVQ PGRSLRLSCA ASGFTFSSRG MHWVRQAPGK GLEWVAVIGY DGQEKYYADS VKGRFTISRD NSKNTLYLQM NSLRAEDTAV YYCVKGPLQE PPYDYGMDVW GQGTTVTVSS AAALDNEKSN GTIIHVKGKH LCPSPLFPGP SKPFWVLVVV GGVLACYSLL VTVAFIIFWV RSKRSRLLHS DYMNMTPRRP GPTRKHYQPY APPRDFAAYR SRVKFSRSAD APAYQQGQNQ LYNELNLGRR EEYDVLDKRR GRDPEMGGKP RRKNPQEGLY NELQKDKMAE AYSEIGMKGE RRRGKGHDGL YQGLSTATKD TYDALHMQAL PPR.

It will be appreciated that the sequences recited herein can be useful by themselves, in combination with one or more sequences recited herein, and/or incorporated into cells (such as CAR or TCR-based T cells) for use in immune- or other therapies. It will be further appreciated that these sequences can be used in accordance with the invention incorporated in vectors for transduction, transfection, and the like, into cells.

It will be appreciated that adverse events may be minimized by transducing the immune cells (containing one or more CARs or TCRs) with a suicide gene. It may also be desired to incorporate an inducible “on” or “accelerator” switch into the immune cells. Suitable techniques include use of inducible caspase-9 (U.S. Appl. 2011/0286980) or a thymidine kinase, before, after or at the same time, as the cells are transduced with the CAR construct of the present invention. Additional methods for introducing suicide genes and/or “on” switches include TALENS, zinc fingers, RNAi, siRNA, shRNA, antisense technology, and other techniques known in the art.

In accordance with the invention, additional on-off or other types of control switch techniques may be incorporated herein. These techniques may employ the use of dimerization domains and optional activators of such domain dimerization. These techniques include, e.g., those described by Wu et al., Science 2014 350 (6258) utilizing FKBP/Rapalog dimerization systems in certain cells, the contents of which are incorporated by reference herein in their entirety. Additional dimerization technology is described in, e.g., Fegan et al. Chem. Rev. 2010, 110, 3315-3336 as well as U.S. Pat. Nos. 5,830,462; 5,834,266; 5,869,337; and 6,165,787, the contents of which are also incorporated by reference herein in their entirety. Additional dimerization pairs may include cyclosporine-A/cyclophilin, receptor, estrogen/estrogen receptor (optionally using tamoxifen), glucocorticoids/glucocorticoid receptor, tetracycline/tetracycline receptor, vitamin D/vitamin D receptor. Further examples of dimerization technology can be found in e.g., WO2014/127261, WO2015/090229, US2014/0286987, US2015/0266973, US2016/0046700, U.S. Pat. No. 8,486,693, US2014/0171649, and US2012/0130076, the contents of which are further incorporated by reference herein in their entirety.

IV. Vectors, Cells, and Pharmaceutical Compositions

In certain aspects, provided herein are vectors comprising a polynucleotide of the present invention. In some embodiments, the present invention is directed to a vector or a set of vectors comprising a polynucleotide encoding a CAR or a TCR, as described herein. In other embodiments, the present invention is directed to a vector or a set of vectors comprising a polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as disclosed herein.

Any vector known in the art can be suitable for the present invention. In some embodiments, the vector is a viral vector. In some embodiments, the vector is a retroviral vector (such as pMSVG1), a DNA vector, a murine leukemia virus vector, an SFG vector, a plasmid, a RNA vector, an adenoviral vector, a baculoviral vector, an Epstein Barr viral vector, a papovaviral vector, a vaccinia viral vector, a herpes simplex viral vector, an adenovirus associated vector (AAV), a lentiviral vector (such as pGAR), or any combination thereof.

The pGAR sequence (SEQ ID NO: 413) is as follows:

CTGACGCGCCCTGTAGCGGCGCATTAAGCGCGGCGGGTGTGGTGGTTACGCGCAGCGT GACCGCTACACTTGCCAGCGCCCTAGCGCCCGCTCCTTTCGCTTTCTTCCCTTCCTTT CTCGCCACGTTCGCCGGCTTTCCCCGTCAAGCTCTAAATCGGGGGCTCCCTTTAGGGT TCCGATTTAGTGCTTTACGGCACCTCGACCCCAAAAAACTTGATTAGGGTGATGGTTC ACGTAGTGGGCCATCGCCCTGATAGACGGTTTTTCGCCCTTTGACGTTGGAGTCCACG TTCTTTAATAGTGGACTCTTGTTCCAAACTGGAACAACACTCAACCCTATCTCGGTCT ATTCTTTTGATTTATAAGGGATTTTGCCGATTTCGGCCTATTGGTTAAAAAATGAGCT GATTTAACAAAAATTTAACGCGAATTTTAACAAAATATTAACGCTTACAATTTGCCAT TCGCCATTCAGGCTGCGCAACTGTTGGGAAGGGCGATCGGTGCGGGCCTCTTCGCTAT TACGCCAGCTGGCGAAAGGGGGATGTGCTGCAAGGCGATTAAGTTGGGTAACGCCAGG GTTTTCCCAGTCACGACGTTGTAAAACGACGGCCAGTGAATTGTAATACGACTCACTA TAGGGCGACCCGGGGATGGCGCGCCAGTAATCAATTACGGGGTCATTAGTTCATAGCC CATATATGGAGTTCCGCGTTACATAACTTACGGTAAATGGCCCGCCTGGCTGACCGCC CAACGACCCCCGCCCATTGACGTCAATAATGACGTATGTTCCCATAGTAACGCCAATA GGGACTTTCCATTGACGTCAATGGGTGGAGTATTTACGGTAAACTGCCCACTTGGCAG TACATCAAGTGTATCATATGCCAAGTACGCCCCCTATTGACGTCAATGACGGTAAATG GCCCGCCTGGCATTATGCCCAGTACATGACCTTATGGGACTTTCCTACTTGGCAGTAC ATCTACGTATTAGTCATCGCTATTACCATGCTGATGCGGTTTTGGCAGTACATCAATG GGCGTGGATAGCGGTTTGACTCACGGGGATTTCCAAGTCTCCACCCCATTGACGTCAA TGGGAGTTTGTTTTGGCACCAAAATCAACGGGACTTTCCAAAATGTCGTAACAACTCC GCCCCATTGACGCAAATGGGCGGTAGGCGTGTACGGTGGGAGGTCTATATAAGCAGAG CTGGTTTAGTGAACCGGGGTCTCTCTGGTTAGACCAGATCTGAGCCTGGGAGCTCTCT GGCTAACTAGGGAACCCACTGCTTAAGCCTCAATAAAGCTTGCCTTGAGTGCTTCAAG TAGTGTGTGCCCGTCTGTTGTGTGACTCTGGTAACTAGAGATCCCTCAGACCCTTTTA GTCAGTGTGGAAAATCTCTAGCAGTGGCGCCCGAACAGGGACTTGAAAGCGAAAGGGA AACCAGAGGAGCTCTCTCGACGCAGGACTCGGCTTGCTGAAGCGCGCACGGCAAGAGG CGAGGGGCGGCGACTGGTGAGTACGCCAAAAATTTTGACTAGCGGAGGCTAGAAGGAG AGAGATGGGTGCGAGAGCGTCAGTATTAAGCGGGGGAGAATTAGATCGCGATGGGAAA AAATTCGGTTAAGGCCAGGGGGAAAGAAAAAATATAAATTAAAACATATAGTATGGGC AAGCAGGGAGCTAGAACGATTCGCAGTTAATCCTGGCCTGTTAGAAACATCAGAAGGC TGTAGACAAATACTGGGACAGCTACAACCATCCCTTCAGACAGGATCAGAAGAACTTA GATCATTATATAATACAGTAGCAACCCTCTATTGTGTGCATCAAAGGATAGAGATAAA AGACACCAAGGAAGCTTTAGACAAGATAGAGGAAGAGCAAAACAAAAGTAAGACCACC GCACAGCAAGCCGCCGCTGATCTTCAGACCTGGAGGAGGAGATATGAGGGACAATTGG AGAAGTGAATTATATAAATATAAAGTAGTAAAAATTGAACCATTAGGAGTAGCACCCA CCAAGGCAAAGAGAAGAGTGGTGCAGAGAGAAAAAAGAGCAGTGGGAATAGGAGCTTT GTTCCTTGGGTTCTTGGGAGCAGCAGGAAGCACTATGGGCGCAGCGTCAATGACGCTG ACGGTACAGGCCAGACAATTATTGTCTGGTATAGTGCAGCAGCAGAACAATTTGCTGA GGGCTATTGAGGCGCAACAGCATCTGTTGCAACTCACAGTCTGGGGCATCAAGCAGCT CCAGGCAAGAATCCTGGCTGTGGAAAGATACCTAAAGGATCAACAGCTCCTGGGGATT TGGGGTTGCTCTGGAAAACTCATTTGCACCACTGCTGTGCCTTGGAATGCTAGTTGGA GTAATAAATCTCTGGAACAGATTTGGAATCACACGACCTGGATGGAGTGGGACAGAGA AATTAACAATTACACAAGCTTAATACACTCCTTAATTGAAGAATCGCAAAACCAGCAA GAAAAGAATGAACAAGAATTATTGGAATTAGATAAATGGGCAAGTTTGTGGAATTGGT TTAACATAACAAATTGGCTGTGGTATATAAAATTATTCATAATGATAGTAGGAGGCTT GGTAGGTTTAAGAATAGTTTTTGCTGTACTTTCTATAGTGAATAGAGTTAGGCAGGGA TATTCACCATTATCGTTTCAGACCCACCTCCCAACCCCGAGGGGACCCGACAGGCCCG AAGGAATAGAAGAAGAAGGTGGAGAGAGAGACAGAGACAGATCCATTCGATTAGTGAA CGGATCTCGACGGTATCGGTTAACTTTTAAAAGAAAAGGGGGGATTGGGGGGTACAGT GCAGGGGAAAGAATAGTAGACATAATAGCAACAGACATACAAACTAAAGAATTACAAA AACAAATTACAAAATTCAAAATTTTATCGCGATCGCGGAATGAAAGACCCCACCTGTA GGTTTGGCAAGCTAGCTTAAGTAACGCCATTTTGCAAGGCATGGAAAATACATAACTG AGAATAGAGAAGTTCAGATCAAGGTTAGGAACAGAGAGACAGCAGAATATGGGCCAAA CAGGATATCTGTGGTAAGCAGTTCCTGCCCCGGCTCAGGGCCAAGAACAGATGGTCCC CAGATGCGGTCCCGCCCTCAGCAGTTTCTAGAGAACCATCAGATGTTTCCAGGGTGCC CCAAGGACCTGAAAATGACCCTGTGCCTTATTTGAACTAACCAATCAGTTCGCTTCTC GCTTCTGTTCGCGCGCTTCTGCTCCCCGAGCTCAATAAAAGAGCCCACAACCCCTCAC TCGGCGCGCCAGTCCTTCGAAGTAGATCTTTGTCGATCCTACCATCCACTCGACACAC CCGCCAGCGGCCGCTGCCAAGCTTCCGAGCTCTCGAATTAATTCACGGTACCCACCAT GGCCTAGGGAGACTAGTCGAATCGATATCAACCTCTGGATTACAAAATTTGTGAAAGA TTGACTGGTATTCTTAACTATGTTGCTCCTTTTACGCTATGTGGATACGCTGCTTTAA TGCCTTTGTATCATGCTATTGCTTCCCGTATGGCTTTCATTTTCTCCTCCTTGTATAA ATCCTGGTTGCTGTCTCTTTATGAGGAGTTGTGGCCCGTTGTCAGGCAACGTGGCGTG GTGTGCACTGTGTTTGCTGACGCAACCCCCACTGGTTGGGGCATTGCCACCACCTGTC AGCTCCTTTCCGGGACTTTCGCTTTCCCCCTCCCTATTGCCACGGCGGAACTCATCGC CGCCTGCCTTGCCCGCTGCTGGACAGGGGCTCGGCTGTTGGGCACTGACAATTCCGTG GTGTTGTCGGGGAAGCTGACGTCCTTTTCATGGCTGCTCGCCTGTGTTGCCACCTGGA TTCTGCGCGGGACGTCCTTCTGCTACGTCCCTTCGGCCCTCAATCCAGCGGACCTTCC TTCCCGCGGCCTGCTGCCGGCTCTGCGGCCTCTTCCGCGTCTTCGCCTTCGCCCTCAG ACGAGTCGGATCTCCCTTTGGGCCGCCTCCCCGCCTGGTTAATTAAAGTACCTTTAAG ACCAATGACTTACAAGGCAGCTGTAGATCTTAGCCACTTTTTAAAAGAAAAGGGGGGA CTGGAAGGGCGAATTCACTCCCAACGAAGACAAGATCTGCTTTTTGCTTGTACTGGGT CTCTCTGGTTAGACCAGATCTGAGCCTGGGAGCTCTCTGGCTAACTAGGGAACCCACT GCTTAAGCCTCAATAAAGCTTGCCTTGAGTGCTTCAAGTAGTGTGTGCCCGTCTGTTG TGTGACTCTGGTAACTAGAGATCCCTCAGACCCTTTTAGTCAGTGTGGAAAATCTCTA GCAGGCATGCCAGACATGATAAGATACATTGATGAGTTTGGACAAACCACAACTAGAA TGCAGTGAAAAAAATGCTTTATTTGTGAAATTTGTGATGCTATTGCTTTATTTGTAAC CATTATAAGCTGCAATAAACAAGTTAACAACAACAATTGCATTCATTTTATGTTTCAG GTTCAGGGGGAGGTGTGGGAGGTTTTTTGGCGCGCCATCGTCGAGGTTCCCTTTAGTG AGGGTTAATTGCGAGCTTGGCGTAATCATGGTCATAGCTGTTTCCTGTGTGAAATTGT TATCCGCTCACAATTCCACACAACATACGAGCCGGAAGCATAAAGTGTAAAGCCTGGG GTGCCTAATGAGTGAGCTAACTCACATTAATTGCGTTGCGCTCACTGCCCGCTTTCCA GTCGGGAAACCTGTCGTGCCAGCTGCATTAATGAATCGGCCAACGCGCGGGGAGAGGC GGTTTGCGTATTGGGCGCTCTTCCGCTTCCTCGCTCACTGACTCGCTGCGCTCGGTCG TTCGGCTGCGGCGAGCGGTATCAGCTCACTCAAAGGCGGTAATACGGTTATCCACAGA ATCAGGGGATAACGCAGGAAAGAACATGTGAGCAAAAGGCCAGCAAAAGGCCAGGAAC CGTAAAAAGGCCGCGTTGCTGGCGTTTTTCCATAGGCTCCGCCCCCCTGACGAGCATC ACAAAAATCGACGCTCAAGTCAGAGGTGGCGAAACCCGACAGGACTATAAAGATACCA GGCGTTTCCCCCTGGAAGCTCCCTCGTGCGCTCTCCTGTTCCGACCCTGCCGCTTACC GGATACCTGTCCGCCTTTCTCCCTTCGGGAAGCGTGGCGCTTTCTCATAGCTCACGCT GTAGGTATCTCAGTTCGGTGTAGGTCGTTCGCTCCAAGCTGGGCTGTGTGCACGAACC CCCCGTTCAGCCCGACCGCTGCGCCTTATCCGGTAACTATCGTCTTGAGTCCAACCCG GTAAGACACGACTTATCGCCACTGGCAGCAGCCACTGGTAACAGGATTAGCAGAGCGA GGTATGTAGGCGGTGCTACAGAGTTCTTGAAGTGGTGGCCTAACTACGGCTACACTAG AAGAACAGTATTTGGTATCTGCGCTCTGCTGAAGCCAGTTACCTTCGGAAAAAGAGTT GGTAGCTCTTGATCCGGCAAACAAACCACCGCTGGTAGCGGTGGTTTTTTTGTTTGCA AGCAGCAGATTACGCGCAGAAAAAAAGGATCTCAAGAAGATCCTTTGATCTTTTCTAC GGGGTCTGACGCTCAGTGGAACGAAAACTCACGTTAAGGGATTTTGGTCATGAGATTA TCAAAAAGGATCTTCACCTAGATCCTTTTAAATTAAAAATGAAGTTTTAAATCAATCT AAAGTATATATGAGTAAACTTGGTCTGACAGTTACCAATGCTTAATCAGTGAGGCACC TATCTCAGCGATCTGTCTATTTCGTTCATCCATAGTTGCCTGACTCCCCGTCGTGTAG ATAACTACGATACGGGAGGGCTTACCATCTGGCCCCAGTGCTGCAATGATACCGCGAG ACCCACGCTCACCGGCTCCAGATTTATCAGCAATAAACCAGCCAGCCGGAAGGGCCGA GCGCAGAAGTGGTCCTGCAACTTTATCCGCCTCCATCCAGTCTATTAATTGTTGCCGG GAAGCTAGAGTAAGTAGTTCGCCAGTTAATAGTTTGCGCAACGTTGTTGCCATTGCTA CAGGCATCGTGGTGTCACGCTCGTCGTTTGGTATGGCTTCATTCAGCTCCGGTTCCCA ACGATCAAGGCGAGTTACATGATCCCCCATGTTGTGCAAAAAAGCGGTTAGCTCCTTC GGTCCTCCGATCGTTGTCAGAAGTAAGTTGGCCGCAGTGTTATCACTCATGGTTATGG CAGCACTGCATAATTCTCTTACTGTCATGCCATCCGTAAGATGCTTTTCTGTGACTGG TGAGTACTCAACCAAGTCATTCTGAGAATAGTGTATGCGGCGACCGAGTTGCTCTTGC CCGGCGTCAATACGGGATAATACCGCGCCACATAGCAGAACTTTAAAAGTGCTCATCA TTGGAAAACGTTCTTCGGGGCGAAAACTCTCAAGGATCTTACCGCTGTTGAGATCCAG TTCGATGTAACCCACTCGTGCACCCAACTGATCTTCAGCATCTTTTACTTTCACCAGC GTTTCTGGGTGAGCAAAAACAGGAAGGCAAAATGCCGCAAAAAAGGGAATAAGGGCGA CACGGAAATGTTGAATACTCATACTCTTCCTTTTTCAATATTATTGAAGCATTTATCA GGGTTATTGTCTCATGAGCGGATACATATTTGAATGTATTTAGAAAAATAAACAAATA GGGGTTCCGCGCACATTTCCCCGAAAAGTGCCAC.

The pGAR vector map is set forth in FIG. 19 .

Suitable additional exemplary vectors include e.g., pBABE-puro, pBABE-neo largeTcDNA, pBABE-hygro-hTERT, pMKO.1 GFP, MSCV-IRES-GFP, pMSCV PIG (Puro IRES GFP empty plasmid), pMSCV-loxp-dsRed-loxp-eGFP-Puro-WPRE, MSCV IRES Luciferase, pMIG, MDH1-PGK-GFP_2.0, TtRMPVIR, pMSCV-IRES-mCherry FP, pRetroX GFP T2A Cre, pRXTN, pLncEXP, and pLXIN-Luc.

In other aspects, provided herein are cells comprising a polynucleotide or a vector of the present invention. In some embodiments, the present invention is directed to cells, in vitro cells, comprising a polynucleotide encoding a CAR or a TCR, as described herein. In some embodiments, the present invention is directed to cells, e.g., in vitro cells, comprising a polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as disclosed herein. In other embodiments, the present invention is directed to in vitro cells comprising a polypeptide encoded by a polynucleotide encoding a CAR or a TCR, as disclosed herein. In other embodiments, the present invention is directed to cells, in vitro cells, comprising a polypeptide encoded by a polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as disclosed herein.

Any cell may be used as a host cell for the polynucleotides, the vectors, or the polypeptides of the present invention. In some embodiments, the cell can be a prokaryotic cell, fungal cell, yeast cell, or higher eukaryotic cells such as a mammalian cell. Suitable prokaryotic cells include, without limitation, eubacteria, such as Gram-negative or Gram-positive organisms, for example, Enterobactehaceae such as Escherichia, e.g., E. coli; Enterobacter; Erwinia; Klebsiella; Proteus; Salmonella, e.g., Salmonella typhimurium; Serratia, e.g., Serratia marcescans, and Shigella; Bacilli such as B. subtilis and B. licheniformis; Pseudomonas such as P. aeruginosa; and Streptomyces. In some embodiments, the cell is a human cell. In some embodiments, the cell is an immune cell. In some embodiments, the immune cell is selected from the group consisting of a T cell, a B cell, a tumor infiltrating lymphocyte (TIL), a TCR expressing cell, a natural killer (NK) cell, a dendritic cell, a granulocyte, an innate lymphoid cell, a megakaryocyte, a monocyte, a macrophage, a platelet, a thymocyte, and a myeloid cell. In one embodiment, the immune cell is a T cell. In another embodiment, the immune cell is an NK cell. In certain embodiments, the T cell is a tumor-infiltrating lymphocyte (TIL), autologous T cell, engineered autologous T cell (eACT™), an allogeneic T cell, a heterologous T cell, or any combination thereof.

The cell of the present invention can be obtained through any source known in the art. For example, T cells can be differentiated in vitro from a hematopoietic stem cell population, or T cells can be obtained from a subject. T cells can be obtained from, e.g., peripheral blood mononuclear cells, bone marrow, lymph node tissue, cord blood, thymus tissue, tissue from a site of infection, ascites, pleural effusion, spleen tissue, and tumors. In addition, the T cells can be derived from one or more T cell lines available in the art. T cells can also be obtained from a unit of blood collected from a subject using any number of techniques known to the skilled artisan, such as FICOLL™ separation and/or apheresis. In certain embodiments, the cells collected by apheresis are washed to remove the plasma fraction, and placed in an appropriate buffer or media for subsequent processing. In some embodiments, the cells are washed with PBS. As will be appreciated, a washing step can be used, such as by using a semiautomated flowthrough centrifuge, e.g., the COBE™ 2991 cell processor, the Baxter CYTOMATE™, or the like. In some embodiments, the washed cells are resuspended in one or more biocompatible buffers, or other saline solution with or without buffer. In certain embodiments, the undesired components of the apheresis sample are removed. Additional methods of isolating T cells for a T cell therapy are disclosed in U.S. Patent Publication No. 2013/0287748, which is herein incorporated by references in its entirety.

In certain embodiments, T cells are isolated from PBMCs by lysing the red blood cells and depleting the monocytes, e.g., by using centrifugation through a PERCOLL™ gradient. In some embodiments, a specific subpopulation of T cells, such as CD28⁺, CD4⁺, CD8⁺, CD45RA⁺, and CD45RO⁺ T cells is further isolated by positive or negative selection techniques known in the art. For example, enrichment of a T cell population by negative selection can be accomplished with a combination of antibodies directed to surface markers unique to the negatively selected cells. In some embodiments, cell sorting and/or selection via negative magnetic immunoadherence or flow cytometry that uses a cocktail of monoclonal antibodies directed to cell surface markers present on the cells negatively selected can be used. For example, to enrich for CD4⁺ cells by negative selection, a monoclonal antibody cocktail typically includes antibodies to CD14, CD20, CD11b, CD16, HLA-DR, and CD8. In certain embodiments, flow cytometry and cell sorting are used to isolate cell populations of interest for use in the present invention.

In some embodiments, PBMCs are used directly for genetic modification with the immune cells (such as CARs or TCRs) using methods as described herein. In certain embodiments, after isolating the PBMCs, T lymphocytes are further isolated, and both cytotoxic and helper T lymphocytes are sorted into naive, memory, and effector T cell subpopulations either before or after genetic modification and/or expansion.

In some embodiments, CD8⁺ cells are further sorted into naive, central memory, and effector cells by identifying cell surface antigens that are associated with each of these types of CD8⁺ cells. In some embodiments, the expression of phenotypic markers of central memory T cells includes CD45RO, CD62L, CCR7, CD28, CD3, and CD127 and are negative for granzyme B. In some embodiments, central memory T cells are CD45RO⁺, CD62L⁺, CD8⁺ T cells. In some embodiments, effector T cells are negative for CD62L, CCR7, CD28, and CD127 and positive for granzyme B and perforin. In certain embodiments, CD4⁺ T cells are further sorted into subpopulations. For example, CD4⁺ T helper cells can be sorted into naive, central memory, and effector cells by identifying cell populations that have cell surface antigens.

In some embodiments, the immune cells, e.g., T cells, are genetically modified following isolation using known methods, or the immune cells are activated and expanded (or differentiated in the case of progenitors) in vitro prior to being genetically modified. In another embodiment, the immune cells, e.g., T cells, are genetically modified with the chimeric antigen receptors described herein (e.g., transduced with a viral vector comprising one or more nucleotide sequences encoding a CAR) and then are activated and/or expanded in vitro. Methods for activating and expanding T cells are known in the art and are described, e.g., in U.S. Pat. Nos. 6,905,874; 6,867,041; and 6,797,514; and PCT Publication No. WO 2012/079000, the contents of which are hereby incorporated by reference in their entirety. Generally, such methods include contacting PBMC or isolated T cells with a stimulatory agent and costimulatory agent, such as anti-CD3 and anti-CD28 antibodies, generally attached to a bead or other surface, in a culture medium with appropriate cytokines, such as IL-2. Anti-CD3 and anti-CD28 antibodies attached to the same bead serve as a “surrogate” antigen presenting cell (APC). One example is The Dynabeads® system, a CD3 CD28 activator/stimulator system for physiological activation of human T cells. In other embodiments, the T cells are activated and stimulated to proliferate with feeder cells and appropriate antibodies and cytokines using methods such as those described in U.S. Pat. Nos. 6,040,177 and 5,827,642 and PCT Publication No. WO 2012/129514, the contents of which are hereby incorporated by reference in their entirety.

In certain embodiments, the T cells are obtained from a donor subject. In some embodiments, the donor subject is human patient afflicted with a cancer or a tumor. In other embodiments, the donor subject is a human patient not afflicted with a cancer or a tumor.

Other aspects of the present invention are directed to compositions comprising a polynucleotide described herein, a vector described herein, a polypeptide described herein, or an in vitro cell described herein. In some embodiments, the composition comprises a pharmaceutically acceptable carrier, diluent, solubilizer, emulsifier, preservative and/or adjuvant. In some embodiments, the composition comprises an excipient. In one embodiment, the composition comprises a polynucleotide encoding a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA. In another embodiment, the composition comprises a CAR or a TCR encoded by a polynucleotide of the present invention, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA. In another embodiment, the composition comprises a T cell comprising a polynucleotide encoding a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA. In another embodiment, the composition comprises an antibody or an antigen binding molecule thereof encoded by a polynucleotide of the present invention. In another embodiment, the composition comprises an in vitro cell comprising a polynucleotide encoding an antibody or an antigen binding molecule thereof encoded by a polynucleotide of the present invention.

In some embodiments, the composition includes more than one different antigen binding molecule to BMCA. In some embodiments, the composition included more than one antigen binding molecule to BCMA, wherein the antigen binding molecules to BCMA bind more than one epitope. In some embodiments, the antigen binding molecules will not compete with one another for binding to BCMA. In some embodiments, any of the antigen binding molecules provided herein are combined together in a pharmaceutical composition.

In other embodiments, the composition is selected for parenteral delivery, for inhalation, or for delivery through the digestive tract, such as orally. The preparation of such pharmaceutically acceptable compositions is within the ability of one skilled in the art. In certain embodiments, buffers are used to maintain the composition at physiological pH or at a slightly lower pH, typically within a pH range of from about 5 to about 8. In certain embodiments, when parenteral administration is contemplated, the composition is in the form of a pyrogen-free, parenterally acceptable aqueous solution comprising a desired antigen binding molecule to BCMA, with or without additional therapeutic agents, in a pharmaceutically acceptable vehicle. In certain embodiments, the vehicle for parenteral injection is sterile distilled water in which an antigen binding molecule to BCMA, with or without at least one additional therapeutic agent, is formulated as a sterile, isotonic solution, properly preserved. In certain embodiments, the preparation involves the formulation of the desired molecule with polymeric compounds (such as polylactic acid or polyglycolic acid), beads or liposomes, that provide for the controlled or sustained release of the product, which are then be delivered via a depot injection. In certain embodiments, implantable drug delivery devices are used to introduce the desired molecule.

V. Methods of the Invention

Another aspect of the invention is directed to a method of making a cell expressing a CAR or a TCR comprising transducing a cell with a polynucleotide disclosed herein under suitable conditions. In some embodiments, the method comprises transducing a cell with a polynucleotide encoding a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA, as disclosed herein. In some embodiments, the method comprises transducing a cell with a vector comprising the polynucleotide encoding a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA. In other embodiments, the method comprises transducing a cell with a polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as disclosed herein. In some embodiments, the method comprises transducing a cell with a vector comprising the polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as described herein. In some embodiments, the method further comprises isolating the cell.

Another aspect of the present invention is directed to a method of inducing an immunity against a tumor comprising administering to a subject an effective amount of a cell comprising a polynucleotide described herein, a vector described herein, or a CAR or a TCR described herein. In one embodiment, the method comprises administering to a subject an effective amount of a cell comprising a polynucleotide encoding a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA, as disclosed herein. In another embodiment, the method comprises administering to a subject an effective amount of a cell comprising a vector comprising a polynucleotide encoding a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA, as disclosed herein. In another embodiment, the method comprises administering to a subject an effective amount of a cell comprising a CAR or a TCR encoded by a polynucleotide disclosed herein, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA. In other embodiments, the method comprises administering to a subject an effective amount of a cell comprising a polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as disclosed herein. In another embodiment, the method comprises administering to a subject an effective amount of a cell comprising a vector comprising a polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as disclosed herein. In another embodiment, the method comprises administering to a subject an effective amount of a cell comprising an antibody or antigen binding molecule thereof encoded by a polynucleotide disclosed herein, wherein the antibody or antigen binding molecule thereof specifically binds to BCMA.

Another aspect of the present invention is directed to a method of inducing an immune response in a subject comprising administering an effective amount of the engineered immune cells of the present application. In some embodiments, the immune response is a T cell-mediated immune response. In some embodiments, the T cell-mediated immune response is directed against one or more target cells. In some embodiments, the engineered immune cell comprises a CAR or a TCR. In some embodiments, the target cell is a tumor cell.

Another aspect of the present invention is directed to a method for treating or preventing a malignancy, said method comprising administering to a subject in need thereof an effective amount of at least one isolated antigen binding molecule described herein or at least one immune cell, wherein the immune cell comprises at least one CAR, TCR, and/or an isolated antigen binding molecule as described herein.

Another aspect of the present invention is directed to a method of treating a hyperproliferative disorder or an inflammatory disease in a subject in need thereof comprising administering to the subject a polynucleotide disclosed herein, a vector disclosed herein, a CAR or a TCR disclosed herein, a cell disclosed herein, or a composition disclosed herein. In some embodiments, the inflammatory disease is selected from the group consisting of rheumatoid arthritis, psoriasis, allergies, asthma, autoimmune diseases such as Crohn's, IBD, fibromyalga, mastocytosis, Celiac disease, and any combination thereof. Additionally, the present invention may be useful to treat diabetes, particularly Type 1 diabetes.

Another aspect of the present invention is directed to a method of treating a cancer in a subject in need thereof comprising administering to the subject a polynucleotide disclosed herein, a vector disclosed herein, a CAR or a TCR disclosed herein, a cell disclosed herein, or a composition disclosed herein. In one embodiment, the method comprises administering a polynucleotide encoding a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA, as disclosed herein. In another embodiment, the method comprises administering a vector comprising a polynucleotide encoding a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA, as disclosed herein. In another embodiment, the method comprises administering a CAR or a TCR encoded by a polynucleotide disclosed herein, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA. In another embodiment, the method comprises administering a cell comprising the polynucleotide, or a vector comprising the polynucleotide, encoding a CAR or a TCR, wherein the CAR or the TCR comprises an antigen binding molecule that specifically binds to BCMA, as disclosed herein. In other embodiments, the method comprises administering a polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as disclosed herein. In another embodiment, the method comprises administering a vector comprising a polynucleotide encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as disclosed herein. In another embodiment, the method comprises administering an antibody or an antigen binding molecule thereof encoded by a polynucleotide disclosed herein, wherein the antibody or the antigen binding molecule thereof specifically binds to BCMA. In another embodiment, the method comprises administering a cell comprising the polynucleotide, or a vector comprising the polynucleotide, encoding an antibody or an antigen binding molecule thereof that specifically binds to BCMA, as disclosed herein.

In some embodiments, an antigen binding molecule to BCMA is administered alone. In certain embodiments, an antigen binding molecule to BCMA is administered as part of a CAR, TCR, or other immune cell. In such immune cells, the antigen binding molecule to BCMA can be under the control of the same promoter region, or a separate promoter. In certain embodiments, the genes encoding protein agents and/or an antigen binding molecule to BCMA can be in separate vectors.

In some embodiments, the methods of treating a cancer in a subject in need thereof comprise a T cell therapy. In one embodiment, the T cell therapy of the present invention is engineered Autologous Cell Therapy (eACT™). According to this embodiment, the method can include collecting blood cells from the patient. The isolated blood cells (e.g., T cells) can then be engineered to express an anti-BCMA CAR of the present invention (“anti-BCMA CAR T cells”). In a particular embodiment, the anti-BCMA CAR T cells are administered to the patient. In some embodiments, the anti-BCMA CAR T cells treat a tumor or a cancer in the patient. In one embodiment the anti-BCMA CAR T cells reduce the size of a tumor or a cancer.

In some embodiments, the donor T cells for use in the T cell therapy are obtained from the patient (e.g., for an autologous T cell therapy). In other embodiments, the donor T cells for use in the T cell therapy are obtained from a subject that is not the patient.

The T cells can be administered at a therapeutically effective amount. For example, a therapeutically effective amount of the T cells can be at least about 10⁴ cells, at least about 10⁵ cells, at least about 10⁶ cells, at least about 10⁷ cells, at least about 10⁸ cells, at least about 10⁹ cells, at least about 10¹⁰ cells, or at least about 10¹¹ cells. In another embodiment, the therapeutically effective amount of the T cells is about 10⁴ cells, about 10⁵ cells, about 10⁶ cells, about 10⁷ cells, or about 10⁸ cells. In one particular embodiment, the therapeutically effective amount of the anti-BCMA CAR T cells is about 2×10⁶ cells/kg, about 3×10⁶ cells/kg, about 4×10⁶ cells/kg, about 5×10⁶ cells/kg, about 6×10⁶ cells/kg, about 7×10⁶ cells/kg, about 8×10⁶ cells/kg, about 9×10⁶ cells/kg, about 1×10⁷ cells/kg, about 2×10⁷ cells/kg, about 3×10⁷ cells/kg, about 4×10⁷ cells/kg, about 5×10⁷ cells/kg, about 6×10⁷ cells/kg, about 7×10⁷ cells/kg, about 8×10⁷ cells/kg, or about 9×10⁷ cells/kg.

Another aspect of the present invention is directed to methods of diagnosis, detection, or validation. In some embodiments, the antigen binding molecule is used as a diagnostic or validation tool. In certain embodiments, the antigen binding molecules disclosed herein are used to assay the amount of BCMA present in a sample and/or subject. In some embodiments, the diagnostic antigen binding molecule is not neutralizing. In some embodiments, the antigen binding molecules disclosed herein are used or provided in an assay kit and/or method for the detection of BCMA in mammalian tissues or cells in order to screen/diagnose for a disease or disorder associated with changes in levels of BCMA. In some embodiments, the kit comprises an antigen binding molecule that binds BCMA, along with means for indicating the binding of the antigen binding molecule with BCMA, if present, and optionally BCMA protein levels. Various means for indicating the presence of an antigen binding molecule can be used. For example, fluorophores, other molecular probes, or enzymes can be linked to the antigen binding molecule and the presence of the antigen binding molecule can be observed in a variety of ways. As will be appreciated by one of skill in the art, the degree of antigen binding molecule binding can be used to determine how much BCMA is in a sample.

V.A. Cancer Treatment

The methods of the invention can be used to treat a cancer in a subject, reduce the size of a tumor, kill tumor cells, prevent tumor cell proliferation, prevent growth of a tumor, eliminate a tumor from a patient, prevent relapse of a tumor, prevent tumor metastasis, induce remission in a patient, or any combination thereof. In certain embodiments, the methods induce a complete response. In other embodiments, the methods induce a partial response.

Cancers that may be treated include tumors that are not vascularized, not yet substantially vascularized, or vascularized. The cancer may also include solid or non-solid tumors. In some embodiments, the cancer is a hematologic cancer. In some embodiments, the cancer is of the white blood cells. In other embodiments, the cancer is of the plasma cells. In some embodiments, the cancer is leukemia, lymphoma, or myeloma. In certain embodiments, the cancer is multiple myeloma, Hodgkin's Disease, non-Hodgkin's lymphoma (NHL), primary mediastinal large B cell lymphoma (PMBC), diffuse large B cell lymphoma (DLBCL), follicular lymphoma (FL), transformed follicular lymphoma, splenic marginal zone lymphoma (SMZL), chronic or acute leukemia, myeloid diseases including but not limited to acute myeloid leukemia (AML), chronic myeloid leukemia (CML), acute lymphoblastic leukemia (ALL) (including non T cell ALL), chronic lymphocytic leukemia (CLL), T-cell lymphoma, one or more of B-cell acute lymphoid leukemia (“BALL”), T-cell acute lymphoid leukemia (“TALL”), acute lymphoid leukemia (ALL), chronic myelogenous leukemia (CML), B cell prolymphocytic leukemia, blastic plasmacytoid dendritic cell neoplasm, Burkitt's lymphoma, diffuse large B cell lymphoma, follicular lymphoma, hairy cell leukemia, small cell- or a large cell-follicular lymphoma, malignant lymphoproliferative conditions, MALT lymphoma, mantle cell lymphoma, Marginal zone lymphoma, myelodysplasia and myelodysplastic syndrome (MDS), hemophagocytic syndrome (Macrophage Activating Syndrome (MAS), and hemophagocytic lymphohistocytosis (HLH)), chronic or acute granulomatous disease, large cell granuloma, leukocyte adhesion deficiency, plasmablastic lymphoma, plasmacytoid dendritic cell neoplasm, Waldenstrom macroglobulinemia, plasma cell proliferative disorders (e.g., asymptomatic myeloma (smoldering multiple myeloma or indolent myeloma), monoclonal gammapathy of undetermined significance (MGUS), plasmacytomas (e.g., plasma cell dyscrasia, solitary myeloma, solitary plasmacytoma, extramedullary plasmacytoma, and multiple plasmacytoma), systemic amyloid light chain amyloidosis, POEMS syndrome (Crow-Fukase syndrome, Takatsuki disease, PEP syndrome), or combinations thereof. In one embodiment, the cancer is a myeloma. In one particular embodiment, the cancer is multiple myeloma.

In some embodiments, the methods further comprise administering a chemotherapeutic. In certain embodiments, the chemotherapeutic selected is a lymphodepleting (preconditioning) chemotherapeutic. Beneficial preconditioning treatment regimens, along with correlative beneficial biomarkers are described in U.S. Provisional Patent Applications 62/262,143 and 62/167,750 which are hereby incorporated by reference in their entirety herein. These describe, e.g., methods of conditioning a patient in need of a T cell therapy comprising administering to the patient specified beneficial doses of cyclophosphamide (between 200 mg/m²/day and 2000 mg/m²/day) and specified doses of fludarabine (between 20 mg/m²/day and 900 mg/m²/day). A preferred dose regimen involves treating a patient comprising administering daily to the patient about 500 mg/m²/day of cyclophosphamide and about 60 mg/m²/day of fludarabine for three days prior to administration of a therapeutically effective amount of engineered T cells to the patient.

In other embodiments, the antigen binding molecule, transduced (or otherwise engineered) cells (such as CARs or TCRs), and the chemotherapeutic agent are administered each in an amount effective to treat the disease or condition in the subject.

In certain embodiments, compositions comprising CAR- and/or TCR-expressing immune effector cells disclosed herein may be administered in conjunction with any number of chemotherapeutic agents. Examples of chemotherapeutic agents include alkylating agents such as thiotepa and cyclophosphamide (CYTOXAN™); alkyl sulfonates such as busulfan, improsulfan and piposulfan; aziridines such as benzodopa, carboquone, meturedopa, and uredopa; ethylenimines and methylamelamines including altretamine, triethylenemelamine, trietylenephosphoramide, triethylenethiophosphaoramide and trimethylolomelamine resume; nitrogen mustards such as chlorambucil, chlornaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, novembichin, phenesterine, prednimustine, trofosfamide, uracil mustard; nitrosureas such as carmustine, chlorozotocin, fotemustine, lomustine, nimustine, ranimustine; antibiotics such as aclacinomysins, actinomycin, authramycin, azaserine, bleomycins, cactinomycin, calicheamicin, carabicin, carminomycin, carzinophilin, chromomycins, dactinomycin, daunorubicin, detorubicin, 6-diazo-5-oxo-L-norleucine, doxorubicin, epirubicin, esorubicin, idarubicin, marcellomycin, mitomycins, mycophenolic acid, nogalamycin, olivomycins, peplomycin, potfiromycin, puromycin, quelamycin, rodorubicin, streptonigrin, streptozocin, tubercidin, ubenimex, zinostatin, zorubicin; anti-metabolites such as methotrexate and 5-fluorouracil (5-FU); folic acid analogues such as denopterin, methotrexate, pteropterin, trimetrexate; purine analogs such as fludarabine, 6-mercaptopurine, thiamiprine, thioguanine; pyrimidine analogs such as ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, dideoxyuridine, doxifluridine, enocitabine, floxuridine, 5-FU; androgens such as calusterone, dromostanolone propionate, epitiostanol, mepitiostane, testolactone; anti-adrenals such as aminoglutethimide, mitotane, trilostane; folic acid replenisher such as frolinic acid; aceglatone; aldophosphamide glycoside; aminolevulinic acid; amsacrine; bestrabucil; bisantrene; edatraxate; defofamine; demecolcine; diaziquone; elformithine; elliptinium acetate; etoglucid; gallium nitrate; hydroxyurea; lentinan; lonidamine; mitoguazone; mitoxantrone; mopidamol; nitracrine; pentostatin; phenamet; pirarubicin; podophyllinic acid; 2-ethylhydrazide; procarbazine; PSK®; razoxane; sizofiran; spirogermanium; tenuazonic acid; triaziquone; 2,2′,2″-trichlorotriethylamine; urethan; vindesine; dacarbazine; mannomustine; mitobronitol; mitolactol; pipobroman; gacytosine; arabinoside (“Ara-C”); cyclophosphamide; thiotepa; taxoids, e.g. paclitaxel (TAXOL™, Bristol-Myers Squibb) and doxetaxel (TAXOTERE®, Rhone-Poulenc Rorer); chlorambucil; gemcitabine; 6-thioguanine; mercaptopurine; methotrexate; platinum analogs such as cisplatin and carboplatin; vinblastine; platinum; etoposide (VP-16); ifosfamide; mitomycin C; mitoxantrone; vincristine; vinorelbine; navelbine; novantrone; teniposide; daunomycin; aminopterin; xeloda; ibandronate; CPT-11; topoisomerase inhibitor RFS2000; difluoromethylomithine (DMFO); retinoic acid derivatives such as Targretin™ (bexarotene), Panretin™, (alitretinoin); ONTAK™ (denileukin diftitox); esperamicins; capecitabine; and pharmaceutically acceptable salts, acids or derivatives of any of the above. In some embodiments, compositions comprising CAR- and/or TCR-expressing immune effector cells disclosed herein may be administered in conjunction with an anti-hormonal agent that acts to regulate or inhibit hormone action on tumors such as anti-estrogens including for example tamoxifen, raloxifene, aromatase inhibiting 4(5)-imidazoles, 4-hydroxytamoxifen, trioxifene, keoxifene, LY117018, onapristone, and toremifene (Fareston); and anti-androgens such as flutamide, nilutamide, bicalutamide, leuprolide, and goserelin; and pharmaceutically acceptable salts, acids or derivatives of any of the above. Combinations of chemotherapeutic agents are also administered where appropriate, including, but not limited to CHOP, i.e., Cyclophosphamide (Cytoxan®), Doxorubicin (hydroxydoxorubicin), Vincristine (Oncovin®), and Prednisone.

In some embodiments, the chemotherapeutic agent is administered at the same time or within one week after the administration of the engineered cell or nucleic acid. In other embodiments, the chemotherapeutic agent is administered from 1 to 4 weeks or from 1 week to 1 month, 1 week to 2 months, 1 week to 3 months, 1 week to 6 months, 1 week to 9 months, or 1 week to 12 months after the administration of the engineered cell or nucleic acid. In some embodiments, the chemotherapeutic agent is administered at least 1 month before administering the cell or nucleic acid. In some embodiments, the methods further comprise administering two or more chemotherapeutic agents.

A variety of additional therapeutic agents may be used in conjunction with the compositions described herein. For example, potentially useful additional therapeutic agents include PD-1 inhibitors such as nivolumab (Opdivo®), pembrolizumab (Keytruda®), pembrolizumab, pidilizumab (CureTech), and atezolizumab (Roche).

Additional therapeutic agents suitable for use in combination with the invention include, but are not limited to, ibrutinib (Imbruvica®), ofatumumab (Arzerra®), rituximab (Rituxan®), bevacizumab (Avastin®), trastuzumab (Herceptin®), trastuzumab emtansine (KADCYLA®), imatinib (Gleevec®), cetuximab (Erbitux®), panitumumab (Vectibix®), catumaxomab, ibritumomab, ofatumumab, tositumomab, brentuximab, alemtuzumab, gemtuzumab, erlotinib, gefitinib, vandetanib, afatinib, lapatinib, neratinib, axitinib, masitinib, pazopanib, sunitinib, sorafenib, toceranib, lestaurtinib, axitinib, cediranib, lenvatinib, nintedanib, pazopanib, regorafenib, semaxanib, sorafenib, sunitinib, tivozanib, toceranib, vandetanib, entrectinib, cabozantinib, imatinib, dasatinib, nilotinib, ponatinib, radotinib, bosutinib, lestaurtinib, ruxolitinib, pacritinib, cobimetinib, selumetinib, trametinib, binimetinib, alectinib, ceritinib, crizotinib, aflibercept, adipotide, denileukin diftitox, mTOR inhibitors such as Everolimus and Temsirolimus, hedgehog inhibitors such as sonidegib and vismodegib, CDK inhibitors such as CDK inhibitor (palbociclib).

In additional embodiments, the composition comprising CAR- and/or TCR-containing immune are administered with an anti-inflammatory agent. Anti-inflammatory agents or drugs can include, but are not limited to, steroids and glucocorticoids (including betamethasone, budesonide, dexamethasone, hydrocortisone acetate, hydrocortisone, hydrocortisone, methylprednisolone, prednisolone, prednisone, triamcinolone), nonsteroidal anti-inflammatory drugs (NSAIDS) including aspirin, ibuprofen, naproxen, methotrexate, sulfasalazine, leflunomide, anti-TNF medications, cyclophosphamide and mycophenolate. Exemplary NSAIDs include ibuprofen, naproxen, naproxen sodium, Cox-2 inhibitors, and sialylates. Exemplary analgesics include acetaminophen, oxycodone, tramadol of proporxyphene hydrochloride. Exemplary glucocorticoids include cortisone, dexamethasone, hydrocortisone, methylprednisolone, prednisolone, or prednisone. Exemplary biological response modifiers include molecules directed against cell surface markers (e.g., CD4, CD5, etc.), cytokine inhibitors, such as the TNF antagonists, (e.g., etanercept (ENBREL®), adalimumab (HUMIRA®) and infliximab (REMICADE®), chemokine inhibitors and adhesion molecule inhibitors. The biological response modifiers include monoclonal antibodies as well as recombinant forms of molecules. Exemplary DMARDs include azathioprine, cyclophosphamide, cyclosporine, methotrexate, penicillamine, leflunomide, sulfasalazine, hydroxychloroquine, Gold (oral (auranofin) and intramuscular), and minocycline.

In certain embodiments, the compositions described herein are administered in conjunction with a cytokine. “Cytokine” as used herein is meant to refer to proteins released by one cell population that act on another cell as intercellular mediators. Examples of cytokines are lymphokines, monokines, and traditional polypeptide hormones. Included among the cytokines are growth hormones such as human growth hormone, N-methionyl human growth hormone, and bovine growth hormone; parathyroid hormone; thyroxine; insulin; proinsulin; relaxin; prorelaxin; glycoprotein hormones such as follicle stimulating hormone (FSH), thyroid stimulating hormone (TSH), and luteinizing hormone (LH); hepatic growth factor (HGF); fibroblast growth factor (FGF); prolactin; placental lactogen; mullerian-inhibiting substance; mouse gonadotropin-associated peptide; inhibin; activin; vascular endothelial growth factor; integrin; thrombopoietin (TPO); nerve growth factors (NGFs) such as NGF-beta; platelet-growth factor; transforming growth factors (TGFs) such as TGF-alpha and TGF-beta; insulin-like growth factor-I and -II; erythropoietin (EPO); osteoinductive factors; interferons such as interferon-alpha, beta, and -gamma; colony stimulating factors (CSFs) such as macrophage-CSF (M-CSF); granulocyte-macrophage-CSF (GM-CSF); and granulocyte-CSF (G-CSF); interleukins (ILs) such as IL-1, IL-1 alpha, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12; IL-15, a tumor necrosis factor such as TNF-alpha or TNF-beta; and other polypeptide factors including LIF and kit ligand (KL). As used herein, the term cytokine includes proteins from natural sources or from recombinant cell culture, and biologically active equivalents of the native sequence cytokines.

All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference. However, the citation of a reference herein should not be construed as an acknowledgement that such reference is prior art to the present invention. To the extent that any of the definitions or terms provided in the references incorporated by reference differ from the terms and discussion provided herein, the present terms and definitions control.

The present invention is further illustrated by the following examples which should not be construed as further limiting. The contents of all references cited throughout this application are expressly incorporated herein by reference.

EXAMPLES Example 1

BCMA expression was measured in various cell lines. BCMA was found to be expressed, with a fragments/kilobase of exon/million reads mapped (FPKM) greater than 35, in 99% of multiple myeloma tumor cell lines tested (FIG. 2A). BCMA expression was greater than that of CD70, CS-1, CLL-1, DLL-1 and FLT3 (FIG. 2A). To further characterize the expression of BCMA, EoL-1 (Sigma), NCI-H929 (Molecular Imaging), and MM1S (Molecular Imaging) cells were stained with an anti-BCMA antibody conjugated to PE (Biolegend, San Diego, Calif.) in stain buffer (BD Pharmingen, San Jose, Calif.) for 30 minutes at 4° C. Cells were then washed and resuspended in stain buffer with propidium iodide (BD Pharmingen) prior to data acquisition. Samples were then acquired by flow cytometry and data analyzed (FIGS. 2B-2C). BCMA expression was observed in the myeloma cell lines MM1S (FIG. 2C) and NCI-H929 (FIG. 2D), but not in the human eosinophil cell line EoL-1 (FIG. 2B). In addition, little to no BCMA expression was observed in normal immune cells (FIG. 2E).

Example 2

A third generation lentiviral transfer vector containing the BCMA CAR constructs was used along with the ViraPower Lentiviral Packaging Mix (Life Technologies, FIX′) to generate the lentiviral supernatants. Briefly, a transfection mix was generated by mixing 15 μg of DNA and 22.5 μl of polyethileneimine (Polysciences, 1 mg/ml) in 600 μl of OptiMEM media. The transfection mix was incubated for 5 minutes at room temperature. Simultaneously, 293T cells (ATCC) were trypsinized and counted. A total of 10×10⁶ total 293T cells were then plated in a T75 flask with the transfection mix. Following culture for three days, supernatants were collected and filtered through a 0.45 μm filter and stored at −80° C.

Peripheral blood mononuclear cells (PBMCs) were isolated from two different healthy donor leukopaks (Hemacare) using ficoll-paque density centrifugation according to the manufacturer's instructions. PBMCs were stimulated using OKT3 (Muromonab-CD3, 50 ng/ml, Miltenyi Biotec) in R10 media supplemented with IL-2 (300 IU/ml, Proleukin®, Prometheus® Therapeutics and Diagnostics). Forty-eight hours post-stimulation, cells were transduced using lentivirus containing the different BCMA CAR constructs at a multiplicity of infection (MOI) of 10. Cells were maintained at 0.5×10⁶-2.0×10⁶ cells/ml prior to use in activity assays.

At day 12 post-stimulation, transduced T cells were stained with recombinant BCMA-Fc (R&D Systems) in stain buffer (BD Pharmingen) for 30 minutes at 4° C. Cells were then washed and stained with goat anti-human IgG Fc PE (Jackson ImmunoResearch, West Grove, Pa.) in stain buffer for 30 minutes at 4° C. Cells were then washed and resuspended in stain buffer with propidium iodide (BD Pharmingen) prior to data acquisition. All experiments were performed in two different donors. BCMA CAR expression was observed for each of the constructs in both Donor 1 (FIG. 3A) and Donor 2 (FIG. 3B) transduced cells.

Effector cells, e.g., anti-BCMA CAR T cells, were cultured with target cells at a 1:1 effector cell to target cell (E:T) ratio in R10 media 12 days after T cell stimulation. Cell lines tested included EoL-1, NCI-H929 and MM1S. Sixteen hours post-co-culture, supernatants were analyzed by Luminex (EMD Millipore), according to the manufacturer's instructions, for production of the cytokines IFNγ (FIGS. 4A-4B), TNFα (FIGS. 4C-4D), and IL-2 (FIGS. 4E-4F). IFNγ (FIGS. 4A-4B), TNFα (FIGS. 4C-4D), and IL-2 (FIGS. 4E-4F) were observed in the supernatant of NCI-H929 and MM1S target cell co-cultures for each anti-BCMA CAR T cell tested in both donors (FIGS. 4A-4B); however, IFNγ (FIGS. 4A-4B), TNFα (FIGS. 4C-4D), and IL-2 (FIGS. 4E-4F) were only observed in the supernatant of EoL-1 target cell co-cultures above background for the IR negative control T cells (FIG. 4A).

Target cell viability was assessed by flow cytometric analysis of propidium iodide (PI) uptake of CD3 negative cells. The anti-BCMA CAR T cells were co-cultured with EoL1 (FIGS. 5A-5B), NCI-H929 (FIGS. 5C-5D), or MM1S (FIGS. 5E-5F) target cells for 16 hours, 40 hours, 64 hours, 88 hours, or 112 hours. Little cytolytic activity was observed in the EoL-1 co-cultures at any time period for the anti-BCMA CAR T cells (FIG. 5A-5B). However, co-culture of the anti-BCMA CAR T cells and the NCI-H929 or MM1S target cells resulted in a decrease in the percentage of viable target cells at each time point measured for each of the anti-BCMA CAR T cells.

To examine proliferation, anti-BCMA CAR T cells were labeled with carboxyfluorescein succinimidyl ester (CFSE) prior to co-culture with EoL-1, NCI-H929, or MM1S target cells at a 1:1 E:T ratio in R10 media. Five days later, T cell proliferation was assessed by flow cytometric analysis of CFSE dilution. Data was analyzed and plotted as histogram using FlowJo™ (FIGS. 6A-6B). All experiments were performed in two different donors.

Example 3

Antigens were biotinylated using the EZ-Link Sulfo-NHS-Biotinylation Kit from Pierce/ThermoFisher (Waltham, Mass.). Goat anti-human F(ab′)2 kappa-FITC (LC-FITC), Extravidin-PE (EA-PE) and streptavidin-633 (SA-633) were obtained from Southern Biotech (Birmingham, Ala.), Sigma (St. Louis, Mo.) and Molecular Probes/Invitrogen (Waltham, Mass.), respectively. Streptavidin MicroBeads and MACS LC separation columns were purchased from Miltenyi Biotec (Gladbachn, Germany).

Naïve Discovery

Eight naïve human synthetic yeast libraries each of ˜109 diversity were propagated as described herein (see WO2009036379, WO2010105256, and WO2012009568 to Xu et al.). For the first two rounds of selection, a magnetic bead sorting technique utilizing the Miltenyi MACs system was performed, as described (Siegel et al., 2004). Briefly, yeast cells (˜1010 cells/library) were incubated with 3 ml of 100 nM biotinylated monomeric antigen or 10 nM biotinylated Fc fusion antigen for 15 minutes at room temperature in FACS wash buffer (phosphate-buffered saline (PBS)/0.1% bovine serum albumin (BSA)). After washing once with 50 ml ice-cold wash buffer, the cell pellet was resuspended in 40 mL wash buffer, and Streptavidin MicroBeads (500 μl) were added to the yeast and incubated for 15 minutes at 4° C. Next, the yeast were pelleted, resuspended in 5 mL wash buffer, and loaded onto a Miltenyi LS column. After the 5 mL was loaded, the column was washed 3 times with 3 ml FACS wash buffer. The column was then removed from the magnetic field, and the yeast were eluted with 5 mL of growth media and then grown overnight. The following rounds of sorting were performed using flow cytometry. Approximately 1×108 yeast were pelleted, washed three times with wash buffer, and incubated with decreasing concentrations of biotinylated monomeric or Fc fusion antigen (100 to 1 nM) under equilibrium conditions at room temperature. Yeast were then washed twice and stained with LC-FITC (diluted 1:100) and either SA-633 (diluted 1:500) or EA-PE (diluted 1:50) secondary reagents for 15 minutes at 4° C. After washing twice with ice-cold wash buffer, the cell pellets were resuspended in 0.4 mL wash buffer and transferred to strainer-capped sort tubes. Sorting was performed using a FACS ARIA sorter (BD Biosciences, San Jose, Calif.) and sort gates were assigned to select for specific binders relative to a background control. Subsequent rounds of selection were focused on reduction of non-specific reagent binders (utilizing soluble membrane proteins from CHO cell), as well as pressuring for affinity to BCMA. After the final round of sorting, yeast were plated and individual colonies were picked for characterization.

Affinity Maturation

Binding optimization of naïve clones was carried out using three maturation strategies: light chain diversification, diversification of VH CDRH1/CDRH2, and performing VHmut/VKmut selections.

Light Chain Diversification: Heavy chain plasmids were extracted and transformed into a light chain library with a diversity of 1×10⁶. Selections were performed as described above with one round of MACS sorting and two rounds of FACS sorting using 10 nM or 1 nM biotinylated antigen for respective rounds.

CDRH1 and CDRH2 Selection: A selected donor CDRH3 was recombined into a premade library with CDRH1 and CDRH2 variants of a diversity of 1×10⁸ and selections were performed as described above. Affinity pressures were applied by incubating the biotinylated antigen-antibody yeast complex with unbiotinylated antigen for varying amounts of time to select for the highest affinity antibodies.

VHmut/VKmut Selection: This round of affinity maturation included error prone PCR-based mutagenesis of the heavy chain and/or light chain. Selections were performed similar to previous cycles, but employing FACS sorting for all selection rounds. Antigen concentration was reduced and cold antigen competition times were increased to pressure further for optimal affinity.

Antibody Production and Purification

Yeast clones were grown to saturation and then induced for 48 h at 30° C. with shaking. After induction, yeast cells were pelleted and the supernatants were harvested for purification. IgGs were purified using a Protein A column and eluted with acetic acid, pH 2.0. Fab fragments were generated by papain digestion and purified over KappaSelect (GE Healthcare LifeSciences, Pittsburgh, Pa.).

ForteBio KD Measurements

ForteBio affinity measurements were performed generally as previously described (Estep et al., 2013). Briefly, ForteBio affinity measurements were performed by loading IgGs on-line onto AHQ sensors. Sensors were equilibrated off-line in assay buffer for 30 minutes and then monitored on-line for 60 seconds for baseline establishment. Sensors with loaded IgGs were exposed to 100 nM antigen for 5 minutes, afterwards they were transferred to assay buffer for 5 minutes for off-rate measurement. Kinetics were analyzed using the 1:1 binding model.

MSD-SET KD Measurements

Equilibrium affinity measurements performed generally as previously described (Estep et al., 2013). Briefly, solution equilibrium titrations (SET) were performed in PBS+0.1% IgG-Free BSA (PBSF) with antigen (BCMA monomer) held constant at 10-100 pM and incubated with 3- to 5-fold serial dilutions of Fab or mAbs starting at 10 pM-10 nM (experimental condition is sample dependent). Antibodies (20 nM in PBS) were coated onto standard bind MSD-ECL plates overnight at 4° C. or at room temperature for 30 minutes. Plates were then blocked by BSA for 30 minutes with shaking at 700 rpm, followed by three washes with wash buffer (PBSF+0.05% Tween 20). SET samples were applied and incubated on the plates for 150 seconds with shaking at 700 rpm followed by one wash. Antigen captured on a plate was detected with 250 ng/mL Sulfotag™-labeled streptavidin in PBSF by incubation on the plate for 3 minutes. The plates were washed three times with wash buffer and then read on the MSD Sector Imager 2400™ instrument using 1× Read Buffer T with surfactant. The percent free antigen was plotted as a function of titrated antibody in Prism™ and fit to a quadratic equation to extract the KD. To improve throughput, liquid handling robots were used throughout MSD-SET experiments, including SET sample preparation.

Octet Red384 Epitope Binning/Ligand Blocking

Epitope binning/ligand blocking was performed using a standard sandwich format cross-blocking assay. Control anti-target IgG was loaded onto AHQ sensors and unoccupied Fc-binding sites on the sensor were blocked with an irrelevant human IgG1 antibody. The sensors were then exposed to 100 nM target antigen followed by a second anti-target antibody or ligand. Data was processed using ForteBio's Data Analysis Software 7.0. Additional binding by the second antibody or ligand after antigen association indicates an unoccupied epitope (non-competitor), while no binding indicates epitope blocking (competitor or ligand blocking).

Size Exclusion Chromatography

A TSKgel SuperSW mAb HTP column (22855) was used for fast SEC analysis of yeast produced mAbs at 0.4 mL/minute with a cycle time of 6 minutes/run. 200 mM Sodium Phosphate and 250 mM Sodium Chloride was used as the mobile phase.

Dynamic Scanning Fluorimetry

10 uL of 20× Sypro Orange™ is added to 20 uL of 0.2-1 mg/mL mAb or Fab solution. A RT-PCR instrument (BioRad CFX96 RT PCR) is used to ramp the sample plate temperature from 40° to 95° C. at 0.5C increment, with 2 minutes to equilibrate at each temperature. The negative of first derivative for the raw data is used to extract Tm.

Clone FS-26528 HC DNA (SEQ ID NO: 271) GAGGTGCAGCTGTTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGTCCCTGAGACTCTC CTGTGCAGCCTCTGGATTCACCTTTGACGACTATGCCATGGCATGGGTCCGCCAGGCTCCAG GGAAGGGGCTGGAGTGGGTCTCAGCTATTAGTGATGCAGGTGACAGAACATACTACGCAGAC TCCGTGAGGGGCCGGTTCACCATCTCCAGAGACAATTCCAAGAACACACTGTATCTGCAAAT GAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCAAGAGCCGAGATGGGAGCCG TATTCGACATATGGGGTCAGGGTACAATGGTCACCGTCTCCTCA Clone FS-26528 HC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 272) EVQLLESGGGLVQPGGSLRLSCAASGFTFDDYAMAWVRQAPGKGLEWVSAISDAGDRTYY ADSVRGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARAEMGAVFDIWGQGTMVTVSS (SEQ ID NO: 273) SCAASGFTFDDYAMA [HC CDR1] (SEQ ID NO: 274) AISDAGDRTYYADSVRG [HC CDR2] (SEQ ID NO: 275) ARAEMGAVFDI [HC CDR3] Clone FS-26528 LC DNA (SEQ ID NO: 276) GAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCT CTCCTGCAGGGCCAGTCAGAGTGTTAGCAGGTACTTAGCCTGGTACCAACAGAAACCTGGCC AGGCTCCCAGGCTCCTCATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTC AGTGGCAGTGGGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATTT TGCAGTTTATTACTGTCAGCAGAGAATCTCCTGGCCTTTCACTTTTGGCGGAGGGACCAAGG TTGAGATCAAACGG Clone FS-26528 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 277) EIVLTQSPATLSLSPGERATLSCRASQSVSRYLAWYQQKPGQAPRLLIYDASNRATGIPARF SGSGSGTDFTLTISSLEPEDFAVYYCQQ RISWPFTFGGGTKVEIKR (SEQ ID NO: 278) RASQSVSRYLA [LC CDR1] (SEQ ID NO: 279) DASNRAT [LC CDR2] (SEQ ID NO: 280) QQRISWPFT [LC CDR3] Clone FS-26528 CAR DNA HxL (SEQ ID NO: 281) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGAGGTGCAGCTGTTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGTCCCTGAGACTCT CCTGTGCAGCCTCTGGATTCACCTTTGACGACTATGCCATGGCATGGGTCCGCCAGGCTCCA GGGAAGGGGCTGGAGTGGGTCTCAGCTATTAGTGATGCAGGTGACAGAACATACTACGCAGA CTCCGTGAGGGGCCGGTTCACCATCTCCAGAGACAATTCCAAGAACACACTGTATCTGCAAA TGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCAAGAGCCGAGATGGGAGCC GTATTCGACATATGGGGTCAGGGTACAATGGTCACCGTCTCCTCAGGGTCTACATCCGGCTC CGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATTGTGTTGACACAGTCTCCAG CCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTT AGCAGGTACTTAGCCTGGTACCAACAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTATGA TGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGACT TCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATTTTGCAGTTTATTACTGTCAGCAGAGA ATCTCCTGGCCTTTCACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGCCGCTGCCCT TGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCAC CCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCT TGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCG CCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACT ACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGA TCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGG ACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCA AACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCT GAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTT GTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGC CACCTAGG Clone FS-26528 CAR HxL (SEQ ID NO: 282) MALPVTALLLPLALLLHAARPEVQLLESGGGLVQPGGSLRLSCAASGFTFDDYAMAWVRQAP GKGLEWVSAISDAGDRTYYADSVRGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARAEMGA VFDIWGQGTMVTVSSGSTSGSGKPGSGEGSTKGEIVLTQSPATLSLSPGERATLSCRASQSV SRYLAWYQQKPGQAPRLLIYDASNRATGIPARFSGSGSGTDFTLTISSLEPEDFAVYYCQQR ISWPFTFGGGTKVEIKRAAALDNEKSNGTIIHVKGKHLCPSPLFPGPSKPFWVLVVVGGVLA CYSLLVTVAFIIFWVRSKRSRLLHSDYMNMTPRRPGPTRKHYQPYAPPRDFAAYRSRVKFSR SADAPAYQQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKPRRKNPQEGLYNELQKDKMA EAYSEIGMKGERRRGKGHDGLYQGLSTATKDTYDALHMQALPPR Clone FS-26528 CAR DNA LxH (SEQ ID NO: 283) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCC TCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGGTACTTAGCCTGGTACCAACAGAAACCTGGC CAGGCTCCCAGGCTCCTCATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTT CAGTGGCAGTGGGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATT TTGCAGTTTATTACTGTCAGCAGAGAATCTCCTGGCCTTTCACTTTTGGCGGAGGGACCAAG GTTGAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTAC AAAGGGGGAGGTGCAGCTGTTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGTCCCTGA GACTCTCCTGTGCAGCCTCTGGATTCACCTTTGACGACTATGCCATGGCATGGGTCCGCCAG GCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGCTATTAGTGATGCAGGTGACAGAACATACTA CGCAGACTCCGTGAGGGGCCGGTTCACCATCTCCAGAGACAATTCCAAGAACACACTGTATC TGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCAAGAGCCGAGATG GGAGCCGTATTCGACATATGGGGTCAGGGTACAATGGTCACCGTCTCCTCAGCCGCTGCCCT TGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCAC CCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCT TGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCG CCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACT ACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGA TCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGG ACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCA AACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCT GAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTT GTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGC CACCTAGG Clone FS-26528 CAR LxH (SEQ ID NO: 284) MALPVTALLLPLALLLHAARPEIVLTQSPATLSLSPGERATLSCRASQSVSRYLAWYQQKPG QAPRLLIYDASNRATGIPARFSGSGSGTDFTLTISSLEPEDFAVYYCQQRISWPFTFGGGTK VEIKRGSTSGSGKPGSGEGSTKGEVQLLESGGGLVQPGGSLRLSCAASGFTFDDYAMAWVRQ APGKGLEWVSAISDAGDRTYYADSVRGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARAEM GAVFDIWGQGTMVTVSSAAALDNEKSNGTIIHVKGKHLCPSPLFPGPSKPFWVLVVVGGVLA CYSLLVTVAFIIFWVRSKRSRLLHSDYMNMTPRRPGPTRKHYQPYAPPRDFAAYRSRVKFSR SADAPAYQQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKPRRKNPQEGLYNELQKDKMA EAYSEIGMKGERRRGKGHDGLYQGLSTATKDTYDALHMQALPPR Clone PC-26534 HC DNA (SEQ ID NO: 285) CAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACTCTC CTGTGCAGCGTCTGGATTCACCTTCAGTGAGCATGGCATGCACTGGGTCCGCCAGGCTCCAG GCAAGGGGCTGGAGTGGGTGGCAGCTATATCTTATGATGGAAGGAATAAACACTATGCAGAC TCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAAT GAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCCAGAGACGGTACTTATCTAG GTGGTCTCTGGTACTTCGACTTATGGGGGAGAGGTACCTTGGTCACCGTCTCCTCA Clone PC-26534 HC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 286) QVQLVESGGGVVQPGRSLRLSCAASGFTFSEHGMHWVRQAPGKGLEWVAAISYDGRNKHY ADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDGTYLGGLWYFDLWGRGTLVTVSS (SEQ ID NO: 287) FTFSEHGMH [HC CDR1] (SEQ ID NO: 288) AISYDGRNKHYADSVKG [HC CDR2] (SEQ ID NO: 289) ARDGTYLGGLWYFDL [HC CDR3] Clone PC-26534 LC DNA (SEQ ID NO: 290) GATATTGTGATGACTCAGTCTCCACTCTCCCTGCCCGTCACCCCTGGAGAGCCGGCCTCCAT CTCCTGCAGGTCTAGTCAGAGCCTCCTGCATAGTAATGGATACAACTATTTGGATTGGTACC TGCAGAAGCCAGGGCAGTCTCCACAGCTCCTGATCTATTTGGGTTCTAATCGGGCCTCCGGG GTCCCTGACAGGTTCAGTGGCAGTGGATCAGGCACAGATTTTACACTGAAAATCAGCAGAGT GGAGGCTGAGGATGTTGGGGTTTATTACTGCATGCAGGGACTCGGCCTCCCTCTCACTTTTG GCGGAGGGACCAAGGTTGAGATCAAACGG Clone PC-26534 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 291) DIVMTQSPLSLPVTPGEPASISCRSSQSLLHSNGYNYLDWYLQKPGQSPQLLIYLGSNRA SGVPDRFSGSGSGTDFTLKISRVEAEDVGVYYCMQGLGLPLTFGGGTKVEIKR (SEQ ID NO: 292) RSSQSLLHSNGYNYLD [LC CDR1] (SEQ ID NO: 293) LGSNRAS [LC CDR2] (SEQ ID NO: 294) MQGLGLPLT [LC CDR3] Clone PC-26534 CAR DNA HxL (SEQ ID NO: 295) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACTCT CCTGTGCAGCGTCTGGATTCACCTTCAGTGAGCATGGCATGCACTGGGTCCGCCAGGCTCCA GGCAAGGGGCTGGAGTGGGTGGCAGCTATATCTTATGATGGAAGGAATAAACACTATGCAGA CTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAA TGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCCAGAGACGGTACTTATCTA GGTGGTCTCTGGTACTTCGACTTATGGGGGAGAGGTACCTTGGTCACCGTCTCCTCAGGGTC TACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGATATTGTGATGA CTCAGTCTCCACTCTCCCTGCCCGTCACCCCTGGAGAGCCGGCCTCCATCTCCTGCAGGTCT AGTCAGAGCCTCCTGCATAGTAATGGATACAACTATTTGGATTGGTACCTGCAGAAGCCAGG GCAGTCTCCACAGCTCCTGATCTATTTGGGTTCTAATCGGGCCTCCGGGGTCCCTGACAGGT TCAGTGGCAGTGGATCAGGCACAGATTTTACACTGAAAATCAGCAGAGTGGAGGCTGAGGAT GTTGGGGTTTATTACTGCATGCAGGGACTCGGCCTCCCTCTCACTTTTGGCGGAGGGACCAA GGTTGAGATCAAACGGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACG TGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTG TTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAAT CTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCAC GCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCC TATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAA CCAACTGTATAACGAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCA GAGGACGGGACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTAT AATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCG GAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTT ATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG Clone PC-26534 CAR HxL (SEQ ID NO: 296) MALPVTALLLPLALLLHAARPQVQLVESGGGVVQPGRSLRLSCAASGFTFSEHGMHWVRQAP GKGLEWVAAISYDGRNKHYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDGTYL GGLWYFDLWGRGTLVTVSSGSTSGSGKPGSGEGSTKGDIVMTQSPLSLPVTPGEPASISCRS SQSLLHSNGYNYLDWYLQKPGQSPQLLIYLGSNRASGVPDRFSGSGSGTDFTLKISRVEAED VGVYYCMQGLGLPLTFGGGTKVEIKRAAALDNEKSNGTIIHVKGKHLCPSPLFPGPSKPFWV LVVVGGVLACYSLLVTVAFIIFWVRSKRSRLLHSDYMNMTPRRPGPTRKHYQPYAPPRDFAA YRSRVKFSRSADAPAYQQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKPRRKNPQEGLY NELQKDKMAEAYSEIGMKGERRRGKGHDGLYQGLSTATKDTYDALHMQALPPR Clone PC-26534 CAR DNA LxH (SEQ ID NO: 297) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGATATTGTGATGACTCAGTCTCCACTCTCCCTGCCCGTCACCCCTGGAGAGCCGGCCTCCA TCTCCTGCAGGTCTAGTCAGAGCCTCCTGCATAGTAATGGATACAACTATTTGGATTGGTAC CTGCAGAAGCCAGGGCAGTCTCCACAGCTCCTGATCTATTTGGGTTCTAATCGGGCCTCCGG GGTCCCTGACAGGTTCAGTGGCAGTGGATCAGGCACAGATTTTACACTGAAAATCAGCAGAG TGGAGGCTGAGGATGTTGGGGTTTATTACTGCATGCAGGGACTCGGCCTCCCTCTCACTTTT GGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAG TGGCGAAGGTAGTACAAAGGGGCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGC CTGGGAGGTCCCTGAGACTCTCCTGTGCAGCGTCTGGATTCACCTTCAGTGAGCATGGCATG CACTGGGTCCGCCAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGCTATATCTTATGATGG AAGGAATAAACACTATGCAGACTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCA AGAACACGCTGTATCTGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGC GCCAGAGACGGTACTTATCTAGGTGGTCTCTGGTACTTCGACTTATGGGGGAGAGGTACCTT GGTCACCGTCTCCTCAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACG TGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTG TTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAAT CTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCAC GCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCC TATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAA CCAACTGTATAACGAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCA GAGGACGGGACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTAT AATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCG GAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTT ATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG Clone PC-26534 CAR LxH (SEQ ID NO: 298) MALPVTALLL PLALLLHAAR PDIVMTQSPL SLPVTPGEPA SISCRSSQSL LHSNGYNYLD WYLQKPGQSP QLLIYLGSNR ASGVPDRFSG SGSGTDFTLK ISRVEAEDVG VYYCMQGLGL PLTFGGGTKV EIKRGSTSGS GKPGSGEGST KGQVQLVESG GGVVQPGRSL RLSCAASGFT FSEHGMHWVR QAPGKGLEWV AAISYDGRNK HYADSVKGRF TISRDNSKNT LYLQMNSLRA EDTAVYYCAR DGTYLGGLWY FDLWGRGTLV TVSSAAALDN EKSNGTIIHV KGKHLCPSPL FPGPSKPFWV LVVVGGVLAC YSLLVTVAFI IFWVRSKRSR LLHSDYMNMT PRRPGPTRKH YQPYAPPRDF AAYRSRVKFS RSADAPAYQQ GQNQLYNELN LGRREEYDVL DKRRGRDPEM GGKPRRKNPQ EGLYNELQKD KMAEAYSEIG MKGERRRGKG HDGLYQGLST ATKDTYDALH MQALPPR Clone AJ-26545 HC DNA (SEQ ID NO: 299) CAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCTCAGTGAAGGTTTC CTGCAGGGCATCTGGATACACCTTCATGGAGCACTATATGCACTGGGTGCGACAGGCCCCTG GACAAGGGCTTGAGTGGATGGGAGTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGCACAG AAGTTCCAGGGCAGAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGGAGCT GAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAGAGAATTGGCCAATGG ACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCA Clone AJ-26545 HC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 300) QVQLVQSGAEVKKPGASVKVSCRASGYTFMEHYMHWVRQAPGQGLEWMGVIGPSGGKTSY AQKFQGRVTMTRDTSTSTVYMELSSLRSEDTAVYYCARESWPMDVWGQGTTVTVSS (SEQ ID NO: 301) YTFMEHYMH (HC CDR1) (SEQ ID NO: 302) VIGPSGGKTSYAQKFQG (HC CDR2) (SEQ ID NO: 303) ARESWPMDV (HC CDR3) Clone AJ-26545 LC DNA (SEQ ID NO: 304) GAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCT CTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCC AGGCTCCCAGGCTCCTCATCTATGGTGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTC AGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATTT TGCAGTTTATTACTGTCAGCAGTACGCCGCCTACCCTACTTTTGGCGGAGGGACCAAGGTTG AGATCAAACGG Clone AJ-26545 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 305) EIVMTQSPATLSVSPGERATLSCRASQSVSSNLAWYQQKPGQAPRLLIYGASTRATGIPARF SGSGSGTEFTLTISSLQSEDFAVYYCQQYAAYPTFGGGTKVEIKR (SEQ ID NO: 306) RASQSVSSNLA (LC CDR1) (SEQ ID NO: 307) GASTRAT (LC CDR2) (SEQ ID NO: 308) QQYAAYPT (LC CDR3) Clone AJ-26545 CAR DNA HxL (SEQ ID NO: 309) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCTCAGTGAAGGTTT CCTGCAGGGCATCTGGATACACCTTCATGGAGCACTATATGCACTGGGTGCGACAGGCCCCT GGACAAGGGCTTGAGTGGATGGGAGTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGCACA GAAGTTCCAGGGCAGAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGGAGC TGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAGAGAATTGGCCAATG GACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCAGGGTCTACATCCGGCTCCGGGAA GCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATAGTGATGACGCAGTCTCCAGCCACCC TGTCTGTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGC AACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTATGGTGCATC CACCAGGGCCACTGGTATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGAGTTCACTC TCACCATCAGCAGCCTGCAGTCTGAAGATTTTGCAGTTTATTACTGTCAGCAGTACGCCGCC TACCCTACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGCCGCTGCCCTTGATAATGA AAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCC CTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCT CTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCA TAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTT ACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGAT GCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGA AGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAGAC GAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTAT TCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGG ACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG Clone AJ-26545 CAR HxL (SEQ ID NO: 310) MALPVTALLL PLALLLHAAR PQVQLVQSGA EVKKPGASVK VSCRASGYTF MEHYMHWVRQ APGQGLEWMG VIGPSGGKTS YAQKFQGRVT MTRDTSTSTV YMELSSLRSE DTAVYYCARE SWPMDVWGQG TTVTVSSGST SGSGKPGSGE GSTKGEIVMT QSPATLSVSP GERATLSCRA SQSVSSNLAW YQQKPGQAPR LLIYGASTRA TGIPARFSGS GSGTEFTLTI SSLQSEDFAV YYCQQYAAYP TFGGGTKVEI KRAAALDNEK SNGTIIHVKG KHLCPSPLFP GPSKPFWVLV VVGGVLACYS LLVTVAFIIF WVRSKRSRLL HSDYMNMTPR RPGPTRKHYQ PYAPPRDFAA YRSRVKFSRS ADAPAYQQGQ NQLYNELNLG RREEYDVLDK RRGRDPEMGG KPRRKNPQEG LYNELQKDKM AEAYSEIGMK GERRRGKGHD GLYQGLSTAT KDTYDALHMQ ALPPR Clone AJ-26545 CAR DNA LxH (SEQ ID NO: 311) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCC TCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGC CAGGCTCCCAGGCTCCTCATCTATGGTGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTT CAGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATT TTGCAGTTTATTACTGTCAGCAGTACGCCGCCTACCCTACTTTTGGCGGAGGGACCAAGGTT GAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAA GGGGCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCTCAGTGAAGG TTTCCTGCAGGGCATCTGGATACACCTTCATGGAGCACTATATGCACTGGGTGCGACAGGCC CCTGGACAAGGGCTTGAGTGGATGGGAGTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGC ACAGAAGTTCCAGGGCAGAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGG AGCTGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAGAGAATTGGCCA ATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCAGCCGCTGCCCTTGATAATGA AAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCC CTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCT CTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCA TAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTT ACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGAT GCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGA AGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAGAC GAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTAT TCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGG ACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG Clone AJ-26545 CAR LxH (SEQ ID NO: 312) MALPVTALLL PLALLLHAAR PEIVMTQSPA TLSVSPGERA TLSCRASQSV SSNLAWYQQK PGQAPRLLIY GASTRATGIP ARFSGSGSGT EFTLTISSLQ SEDFAVYYCQ QYAAYPTFGG GTKVEIKRGS TSGSGKPGSG EGSTKGQVQL VQSGAEVKKP GASVKVSCRA SGYTFMEHYM HWVRQAPGQG LEWMGVIGPS GGKTSYAQKF QGRVTMTRDT STSTVYMELS SLRSEDTAVY YCARESWPMD VWGQGTTVTV SSAAALDNEK SNGTIIHVKG KHLCPSPLFP GPSKPFWVLV VVGGVLACYS LLVTVAFIIF WVRSKRSRLL HSDYMNMTPR RPGPTRKHYQ PYAPPRDFAA YRSRVKFSRS ADAPAYQQGQ NQLYNELNLG RREEYDVLDK RRGRDPEMGG KPRRKNPQEG LYNELQKDKM AEAYSEIGMK GERRRGKGHD GLYQGLSTAT KDTYDALHMQ ALPPR Clone AJ-26554 HC DNA (SEQ ID NO: 313) CAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCTCAGTGAAGGTTTC CTGCAAGGCATCTGGATACACCTTCACGGAGCACTATATGCACTGGGTGCGACAGGCCCCTG GACAAAGGCTTGAGTGGATGGGAGTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGCACAG AAGTTCCAGGGCAGAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGGAGCT GAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAGAGAGTTGGCCAATGG ACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCA Clone AJ-26554 HC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 314) QVQLVQSGAE VKKPGASVKV SCKASGYTFT EHYMHWVRQA PGQRLEWMGV IGPSGGKTSY AQKFQGRVTM TRDTSTSTVY MELSSLRSED TAVYYCARES WPMDVWGQGT TVTVSS (SEQ ID NO: 315) YTFTEHYMH (HC CDR1) (SEQ ID NO: 316) VIGPSGGKTSYAQKFQG (HC CDR2) (SEQ ID NO: 317) ARESWPMDV (HC CDR3) Clone AJ-26554 LC DNA (SEQ ID NO: 318) GAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCT CTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCC AGGCTCCCAGGCTCCTCATCTATGGTGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTC AGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATTT TGCAGTTTATTACTGTCAGCAGTACGCCGCCTACCCTACTTTTGGCGGAGGGACCAAGGTTG AGATCAAACGG Clone AJ-26554 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 319) EIVMTQSPATLSVSPGERATLSCRASQSVSSNLAWYQQKPGQAPRLLIYGASTRATGIPA RFSGSGSGTEFTLTISSLQSEDFAVYYCQQYAAYPTFGGGTKVEIKR (SEQ ID NO: 320) RASQSVSSNLA (LC CDR1) (SEQ ID NO: 321) GASTRAT (LC CDR2) (SEQ ID NO: 322) QQYAAYPT (LC CDR3) Clone AJ-26554 CAR DNA HxL (SEQ ID NO: 323) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCTCAGTGAAGGTTT CCTGCAAGGCATCTGGATACACCTTCACGGAGCACTATATGCACTGGGTGCGACAGGCCCCT GGACAAAGGCTTGAGTGGATGGGAGTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGCACA GAAGTTCCAGGGCAGAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGGAGC TGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAGAGAGTTGGCCAATG GACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCAGGGTCTACATCCGGCTCCGGGAA GCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATAGTGATGACGCAGTCTCCAGCCACCC TGTCTGTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGC AACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTATGGTGCATC CACCAGGGCCACTGGTATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGAGTTCACTC TCACCATCAGCAGCCTGCAGTCTGAAGATTTTGCAGTTTATTACTGTCAGCAGTACGCCGCC TACCCTACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGCCGCTGCCCTTGATAATGA AAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCC CTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCT CTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCA TAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTT ACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGAT GCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGA AGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAGAC GAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTAT TCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGG ACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG Clone AJ-26554 CAR HxL (SEQ ID NO: 324) MALPVTALLL PLALLLHAAR PQVQLVQSGA EVKKPGASVK VSCKASGYTF TEHYMHWVRQ APGQRLEWMG VIGPSGGKTS YAQKFQGRVT MTRDTSTSTV YMELSSLRSE DTAVYYCARE SWPMDVWGQG TTVTVSSGST SGSGKPGSGE GSTKGEIVMT QSPATLSVSP GERATLSCRA SQSVSSNLAW YQQKPGQAPR LLIYGASTRA TGIPARFSGS GSGTEFTLTI SSLQSEDFAV YYCQQYAAYP TFGGGTKVEI KRAAALDNEK SNGTIIHVKG KHLCPSPLFP GPSKPFWVLV VVGGVLACYS LLVTVAFIIF WVRSKRSRLL HSDYMNMTPR RPGPTRKHYQ PYAPPRDFAA YRSRVKFSRS ADAPAYQQGQ NQLYNELNLG RREEYDVLDK RRGRDPEMGG KPRRKNPQEG LYNELQKDKM AEAYSEIGMK GERRRGKGHD GLYQGLSTAT KDTYDALHMQ ALPPR Clone AJ-26554 CAR DNA LxH (SEQ ID NO: 325) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCC TCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGC CAGGCTCCCAGGCTCCTCATCTATGGTGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTT CAGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATT TTGCAGTTTATTACTGTCAGCAGTACGCCGCCTACCCTACTTTTGGCGGAGGGACCAAGGTT GAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAA GGGGCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGGCCTCAGTGAAGG TTTCCTGCAAGGCATCTGGATACACCTTCACGGAGCACTATATGCACTGGGTGCGACAGGCC CCTGGACAAAGGCTTGAGTGGATGGGAGTAATCGGGCCTAGTGGTGGTAAGACAAGCTACGC ACAGAAGTTCCAGGGCAGAGTCACCATGACCAGGGACACGTCCACGAGCACAGTCTACATGG AGCTGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAGAGAGTTGGCCA ATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCAGCCGCTGCCCTTGATAATGA AAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCC CTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCT CTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCA TAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTT ACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGAT GCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGA AGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAGAC GAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTAT TCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGG ACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG Clone AJ-26554 CAR LxH (SEQ ID NO: 326) MALPVTALLL PLALLLHAAR PEIVMTQSPA TLSVSPGERA TLSCRASQSV SSNLAWYQQK PGQAPRLLIY GASTRATGIP ARFSGSGSGT EFTLTISSLQ SEDFAVYYCQ QYAAYPTFGG GTKVEIKRGS TSGSGKPGSG EGSTKGQVQL VQSGAEVKKP GASVKVSCKA SGYTFTEHYM HWVRQAPGQR LEWMGVIGPS GGKTSYAQKF QGRVTMTRDT STSTVYMELS SLRSEDTAVY YCARESWPMD VWGQGTTVTV SSAAALDNEK SNGTIIHVKG KHLCPSPLFP GPSKPFWVLV VVGGVLACYS LLVTVAFIIF WVRSKRSRLL HSDYMNMTPR RPGPTRKHYQ PYAPPRDFAA YRSRVKFSRS ADAPAYQQGQ NQLYNELNLG RREEYDVLDK RRGRDPEMGG KPRRKNPQEG LYNELQKDKM AEAYSEIGMK GERRRGKGHD GLYQGLSTAT KDTYDALHMQ ALPPR Clone NM-26562 HC DNA (SEQ ID NO: 327) CAGGTGCAGCTGCAGGAGTCGGGCCCAGGACTGGTGAAGCCTTCACAGACCCTGTCCCTCAC CTGTACTGTCTCTGGTGGCTCCATCGGGAGTGGTGGTAGTTACTGGAGCTGGATCCGCCAGC ACCCAGGGAAGGGCCTGGAGTGGATTGGGTTGATCTATTACGATGGGAGCACCTACTACAAC CCGTCCCTCAAGAGTCGAGTTACCATATCAGTAGACACGTCTAAGAACCAGTTCTCCCTGAA GCTGAGTTCTGTGACCGCCGCAGACACGGCGGTGTACTACTGCGCCAGAGGCAGGGGATATG AGACTTCTTTAGCCTTCGATATCTGGGGTCAGGGTACAATGGTCACCGTCTCCTCA Clone NM-26562 HC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 328) QVQLQESGPGLVKPSQTLSLTCTVSGGSIGSGGSYWSWIRQHPGKGLEWIGLIYYDGSTY YNPSLKSRVTISVDTSKNQFSLKLSSVTAADTAVYYCARGRGYETSLAFDIWGQGTMVTVSS (SEQ ID NO: 329) GSIGSGGSYWS (HC CDR1) (SEQ ID NO: 330) LIYYDGSTYYNPSLKS (HC CDR2) (SEQ ID NO: 331) ARGRGYETSLAFDI (HC CDR3) Clone NM-26562 LC DNA (SEQ ID NO: 332) GAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCT CTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCTACTTAGCCTGGTACCAACAGAAACCTGGCC AGGCTCCCAGGCTCCTCATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTC AGTGGCAGTGGGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATTT TGCAGTTTATTACTGTCAGCAGAGACACGTCTGGCCTCCTACTTTTGGCGGAGGGACCAAGG TTGAGATCAAACGG Clone NM-26562 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 333) EIVLTQSPATLSLSPGERATLSCRASQSVSSYLAWYQQKPGQAPRLLIYDASNRATGIPA RFSGSGSGTDFTLTISSLEPEDFAVYYCQQRHVWPPTFGGGTKVEIKR (SEQ ID NO: 334) RASQSVSSYLA (LC CDR1) (SEQ ID NO: 335) DASNRAT (LC CDR2) (SEQ ID NO: 336) QQRHVWPPT (LC CDR3) Clone NM-26562 CAR DNA HxL (SEQ ID NO: 337) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GCAGGTGCAGCTGCAGGAGTCGGGCCCAGGACTGGTGAAGCCTTCACAGACCCTGTCCCTCA CCTGTACTGTCTCTGGTGGCTCCATCGGGAGTGGTGGTAGTTACTGGAGCTGGATCCGCCAG CACCCAGGGAAGGGCCTGGAGTGGATTGGGTTGATCTATTACGATGGGAGCACCTACTACAA CCCGTCCCTCAAGAGTCGAGTTACCATATCAGTAGACACGTCTAAGAACCAGTTCTCCCTGA AGCTGAGTTCTGTGACCGCCGCAGACACGGCGGTGTACTACTGCGCCAGAGGCAGGGGATAT GAGACTTCTTTAGCCTTCGATATCTGGGGTCAGGGTACAATGGTCACCGTCTCCTCAGGGTC TACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATTGTGTTGA CACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCC AGTCAGAGTGTTAGCAGCTACTTAGCCTGGTACCAACAGAAACCTGGCCAGGCTCCCAGGCT CCTCATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGT CTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATTTTGCAGTTTATTAC TGTCAGCAGAGACACGTCTGGCCTCCTACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACG GGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACC TCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGT GGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATC CAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCA CAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTG AAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGA GCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTG AGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAG GATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGG GCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACA TGCAAGCCCTGCCACCTAGG Clone NM-26562 CAR HxL (SEQ ID NO: 338) MALPVTALLL PLALLLHAAR PQVQLQESGP GLVKPSQTLS LTCTVSGGSI GSGGSYWSWI RQHPGKGLEW IGLIYYDGST YYNPSLKSRV TISVDTSKNQ FSLKLSSVTA ADTAVYYCAR GRGYETSLAF DIWGQGTMVT VSSGSTSGSG KPGSGEGSTK GEIVLTQSPA TLSLSPGERA TLSCRASQSV SSYLAWYQQK PGQAPRLLIY DASNRATGIP ARFSGSGSGT DFTLTISSLE PEDFAVYYCQ QRHVWPPTFG GGTKVEIKRA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR Clone NM-26562 CAR DNA LxH (SEQ ID NO: 339) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCC TCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCTACTTAGCCTGGTACCAACAGAAACCTGGC CAGGCTCCCAGGCTCCTCATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTT CAGTGGCAGTGGGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATT TTGCAGTTTATTACTGTCAGCAGAGACACGTCTGGCCTCCTACTTTTGGCGGAGGGACCAAG GTTGAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTAC AAAGGGGCAGGTGCAGCTGCAGGAGTCGGGCCCAGGACTGGTGAAGCCTTCACAGACCCTGT CCCTCACCTGTACTGTCTCTGGTGGCTCCATCGGGAGTGGTGGTAGTTACTGGAGCTGGATC CGCCAGCACCCAGGGAAGGGCCTGGAGTGGATTGGGTTGATCTATTACGATGGGAGCACCTA CTACAACCCGTCCCTCAAGAGTCGAGTTACCATATCAGTAGACACGTCTAAGAACCAGTTCT CCCTGAAGCTGAGTTCTGTGACCGCCGCAGACACGGCGGTGTACTACTGCGCCAGAGGCAGG GGATATGAGACTTCTTTAGCCTTCGATATCTGGGGTCAGGGTACAATGGTCACCGTCTCCTC AGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACC TCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGT GGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATC CAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCA CAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTG AAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGA GCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTG AGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAG GATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGG GCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACA TGCAAGCCCTGCCACCTAGG Clone NM-26562 CAR LxH (SEQ ID NO: 340) MALPVTALLL PLALLLHAAR PEIVLTQSPA TLSLSPGERA TLSCRASQSV SSYLAWYQQK PGQAPRLLIY DASNRATGIP ARFSGSGSGT DFTLTISSLE PEDFAVYYCQ QRHVWPPTFG GGTKVEIKRG STSGSGKPGS GEGSTKGQVQ LQESGPGLVK PSQTLSLTCT VSGGSIGSGG SYWSWIRQHP GKGLEWIGLI YYDGSTYYNP SLKSRVTISV DTSKNQFSLK LSSVTAADTA VYYCARGRGY ETSLAFDIWG QGTMVTVSSA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR Clone TS-26564 HC DNA (SEQ ID NO: 341) GAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGTCCCTGAGACTCTC CTGTGCAGCCTCTGGATTCACCTTCAGTAGCTATAGCATGAACTGGGTCCGCCAGGCTCCAG GGAAGGGGCTGGAGTGGGTTTCAACCATTAGTAGTAGTAGTAGTATCATATACTACGCAGAC TCTGTGAAGGGCCGATTCACCATCTCCAGAGACAATGCCAAGAACTCACTGTATCTGCAAAT GAACAGCCTGAGAGCTGAGGACACGGCGGTGTACTACTGCGCCAGAGGTTCTCAGGAGCACC TGATTTTCGATTATTGGGGACAGGGTACATTGGTCACCGTCTCCTCA Clone TS-26564 HC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 342) EVQLVESGGGLVQPGGSLRLSCAASGFTFSSYSMNWVRQAPGKGLEWVSTISSSSSIIYY ADSVKGRFTISRDNAKNSLYLQMNSLRAEDTAVYYCARGSQEHLIFDYWGQGTLVTVSS (SEQ ID NO: 343) FTFSSYSMN (HC CDR1) (SEQ ID NO: 344) TISSSSSIIYYADSVKG (HC CDR2) (SEQ ID NO: 345) ARGSQEHLIFDY (HC CDR3) Clone TS-26564 LC DNA (SEQ ID NO: 346) GAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCT CTCCTGCAGGGCCAGTCAGAGTGTTAGCAGGTACTTAGCCTGGTACCAACAGAAACCTGGCC AGGCTCCCAGGCTCCTCATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTC AGTGGCAGTGGGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATTT TGCAGTTTATTACTGTCAGCAGAGATTCTACTACCCTTGGACTTTTGGCGGAGGGACCAAGG TTGAGATCAAACGG Clone TS-26564 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 347) EIVLTQSPATLSLSPGERATLSCRASQSVSRYLAWYQQKPGQAPRLLIYDASNRATGIPA RFSGSGSGTDFTLTISSLEPEDFAVYYCQQRFYYPWTFGGGTKVEIKR (SEQ ID NO: 348) RASQSVSRYLA (LC CDR1) (SEQ ID NO: 349) DASNRAT (LC CDR2) (SEQ ID NO: 350) QQRFYYPWT (LC CDR3) Clone TS-26564 CAR DNA HxL (SEQ ID NO: 351) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGTCCCTGAGACTCT CCTGTGCAGCCTCTGGATTCACCTTCAGTAGCTATAGCATGAACTGGGTCCGCCAGGCTCCA GGGAAGGGGCTGGAGTGGGTTTCAACCATTAGTAGTAGTAGTAGTATCATATACTACGCAGA CTCTGTGAAGGGCCGATTCACCATCTCCAGAGACAATGCCAAGAACTCACTGTATCTGCAAA TGAACAGCCTGAGAGCTGAGGACACGGCGGTGTACTACTGCGCCAGAGGTTCTCAGGAGCAC CTGATTTTCGATTATTGGGGACAGGGTACATTGGTCACCGTCTCCTCAGGGTCTACATCCGG CTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATTGTGTTGACACAGTCTC CAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGGGCCAGTCAGAGT GTTAGCAGGTACTTAGCCTGGTACCAACAGAAACCTGGCCAGGCTCCCAGGCTCCTCATCTA TGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAG ACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATTTTGCAGTTTATTACTGTCAGCAG AGATTCTACTACCCTTGGACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGCCGCTGC CCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGT CACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTC GCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAG CCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAAC ACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCC AGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCT GGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTG GCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATG GCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGG TTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCC TGCCACCTAGG Clone TS-26564 CAR HxL (SEQ ID NO: 352) MALPVTALLL PLALLLHAAR PEVQLVESGG GLVQPGGSLR LSCAASGFTF SSYSMNWVRQ APGKGLEWVS TISSSSSIIY YADSVKGRFT ISRDNAKNSL YLQMNSLRAE DTAVYYCARG SQEHLIFDYW GQGTLVTVSS GSTSGSGKPG SGEGSTKGEI VLTQSPATLS LSPGERATLS CRASQSVSRY LAWYQQKPGQ APRLLIYDAS NRATGIPARF SGSGSGTDFT LTISSLEPED FAVYYCQQRF YYPWTFGGGT KVEIKRAAAL DNEKSNGTII HVKGKHLCPS PLFPGPSKPF WVLVVVGGVL ACYSLLVTVA FIIFWVRSKR SRLLHSDYMN MTPRRPGPTR KHYQPYAPPR DFAAYRSRVK FSRSADAPAY QQGQNQLYNE LNLGRREEYD VLDKRRGRDP EMGGKPRRKN PQEGLYNELQ KDKMAEAYSE IGMKGERRRG KGHDGLYQGL STATKDTYDA LHMQALPPR Clone TS-26564 CAR DNA LxH (SEQ ID NO: 353) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCC TCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGGTACTTAGCCTGGTACCAACAGAAACCTGGC CAGGCTCCCAGGCTCCTCATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTT CAGTGGCAGTGGGTCTGGGACAGACTTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATT TTGCAGTTTATTACTGTCAGCAGAGATTCTACTACCCTTGGACTTTTGGCGGAGGGACCAAG GTTGAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTAC AAAGGGGGAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGTCCCTGA GACTCTCCTGTGCAGCCTCTGGATTCACCTTCAGTAGCTATAGCATGAACTGGGTCCGCCAG GCTCCAGGGAAGGGGCTGGAGTGGGTTTCAACCATTAGTAGTAGTAGTAGTATCATATACTA CGCAGACTCTGTGAAGGGCCGATTCACCATCTCCAGAGACAATGCCAAGAACTCACTGTATC TGCAAATGAACAGCCTGAGAGCTGAGGACACGGCGGTGTACTACTGCGCCAGAGGTTCTCAG GAGCACCTGATTTTCGATTATTGGGGACAGGGTACATTGGTCACCGTCTCCTCAGCCGCTGC CCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGT CACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTC GCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAG CCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAAC ACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCC AGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCT GGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTG GCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATG GCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGG TTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCC TGCCACCTAGG Clone TS-26564 CAR LxH (SEQ ID NO: 354) MALPVTALLL PLALLLHAAR PEIVLTQSPA TLSLSPGERA TLSCRASQSV SRYLAWYQQK PGQAPRLLIY DASNRATGIP ARFSGSGSGT DFTLTISSLE PEDFAVYYCQ QRFYYPWTFG GGTKVEIKRG STSGSGKPGS GEGSTKGEVQ LVESGGGLVQ PGGSLRLSCA ASGFTFSSYS MNWVRQAPGK GLEWVSTISS SSSIIYYADS VKGRFTISRD NAKNSLYLQM NSLRAEDTAV YYCARGSQEH LIFDYWGQGT LVTVSSAAAL DNEKSNGTII HVKGKHLCPS PLFPGPSKPF WVLVVVGGVL ACYSLLVTVA FIIFWVRSKR SRLLHSDYMN MTPRRPGPTR KHYQPYAPPR DFAAYRSRVK FSRSADAPAY QQGQNQLYNE LNLGRREEYD VLDKRRGRDP EMGGKPRRKN PQEGLYNELQ KDKMAEAYSE IGMKGERRRG KGHDGLYQGL STATKDTYDA LHMQALPPR Clone RY-26568 HC DNA (SEQ ID NO: 355) CAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACTCTC CTGTGCAGCGTCTGGATTCACCTTCGGGAGCTATGGCATGCACTGGGTCCGCCAGGCTCCAG GCAAGGGGCTGGAGTGGGTGGCAGTTATACATTATGATGGAAGTGTTGAATACTATGCAGAC TCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGGACACGCTGTATCTGCAAAT GAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCCAGAACTGACTTCTGGAGCG GATCCCCTCCAAGCTTAGATTACTGGGGACAGGGTACATTGGTCACCGTCTCCTCA Clone RY-26568 HC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 356) QVQLVESGGG VVQPGRSLRL SCAASGFTFG SYGMHWVRQA PGKGLEWVAV IHYDGSVEYY ADSVKGRFTI SRDNSKDTLY LQMNSLRAED TAVYYCARTD FWSGSPPSLD YWGQGTLVTV SS (SEQ ID NO: 357) FTFGSYGMH (HC CDR1) (SEQ ID NO: 358) VIHYDGSVEYYADSVKG (HC CDR2) (SEQ ID NO: 359) ARTDFWSGSPPSLDY (HC CDR3) Clone RY-26568 LC DNA (SEQ ID NO: 360) GACATCCAGTTGACCCAGTCTCCATCTTCCGTGTCTGCATCTGTAGGAGACAGAGTCACCAT CACTTGTCGGGCGAGTCGGGGTATTAGCAGCTGGTTAGCCTGGTATCAGCAGAAACCAGGGA AAGCCCCTAAGCTCCTGATCTATGGTGCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTTC AGCGGCAGTGGATCTGGGACAGATTTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTT TGCAACTTATTACTGTCAGCAGATATACACCTTCCCTTTCACTTTTGGCGGAGGGACCAAGG TTGAGATCAAACGG Clone RY-26568 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 361) DIQLTQSPSSVSASVGDRVTITCRASRGISSWLAWYQQKPGKAPKLLIYGASSLQSGVPSRF SGSGSGTDFTLTISSLQPEDFATYYCQQIYTFPFTFGGGTKVEIKR (SEQ ID NO: 362) RASRGISSWLA (LC CDR1) (SEQ ID NO: 363) GASSLQS (LC CDR2) (SEQ ID NO: 364) QQIYTFPFT (LC CDR3) Clone RY-26568 CAR DNA HxL (SEQ ID NO: 365) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACTCT CCTGTGCAGCGTCTGGATTCACCTTCGGGAGCTATGGCATGCACTGGGTCCGCCAGGCTCCA GGCAAGGGGCTGGAGTGGGTGGCAGTTATACATTATGATGGAAGTGTTGAATACTATGCAGA CTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGGACACGCTGTATCTGCAAA TGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCCAGAACTGACTTCTGGAGC GGATCCCCTCCAAGCTTAGATTACTGGGGACAGGGTACATTGGTCACCGTCTCCTCAGGGTC TACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGACATCCAGTTGA CCCAGTCTCCATCTTCCGTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGTCGGGCG AGTCGGGGTATTAGCAGCTGGTTAGCCTGGTATCAGCAGAAACCAGGGAAAGCCCCTAAGCT CCTGATCTATGGTGCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTTCAGCGGCAGTGGAT CTGGGACAGATTTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTAC TGTCAGCAGATATACACCTTCCCTTTCACTTTTGGCGGAGGGACCAAGGTTGAGATCAAACG GGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACC TCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGT GGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATC CAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCA CAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTG AAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGA GCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTG AGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAG GATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGG GCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACA TGCAAGCCCTGCCACCTAGG Clone RY-26568 CAR HxL  SEQ ID NO: 366) MALPVTALLL PLALLLHAAR PQVQLVESGG GVVQPGRSLR LSCAASGFTF GSYGMHWVRQ APGKGLEWVA VIHYDGSVEY YADSVKGRET ISRDNSKDTL YLQMNSLRAE DTAVYYCART DFWSGSPPSL DYWGQGTLVT VSSGSTSGSG KPGSGEGSTK GDIQLTQSPS SVSASVGDRV TITCRASRGI SSWLAWYQQK PGKAPKLLIY GASSLQSGVP SRFSGSGSGT DFTLTISSLQ PEDFATYYCQ QIYTFPFTFG GGTKVEIKRA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR Clone RY-26568 CAR DNA LxH (SEQ ID NO: 367) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGACATCCAGTTGACCCAGTCTCCATCTTCCGTGTCTGCATCTGTAGGAGACAGAGTCACCA TCACTTGTCGGGCGAGTCGGGGTATTAGCAGCTGGTTAGCCTGGTATCAGCAGAAACCAGGG AAAGCCCCTAAGCTCCTGATCTATGGTGCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTT CAGCGGCAGTGGATCTGGGACAGATTTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATT TTGCAACTTATTACTGTCAGCAGATATACACCTTCCCTTTCACTTTTGGCGGAGGGACCAAG GTTGAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTAC AAAGGGGCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGA GACTCTCCTGTGCAGCGTCTGGATTCACCTTCGGGAGCTATGGCATGCACTGGGTCCGCCAG GCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTTATACATTATGATGGAAGTGTTGAATACTA TGCAGACTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGGACACGCTGTATC TGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGCCAGAACTGACTTC TGGAGCGGATCCCCTCCAAGCTTAGATTACTGGGGACAGGGTACATTGGTCACCGTCTCCTC AGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGCACC TCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTGGGT GGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAGATC CAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCCCCA CAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGGGTG AAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAACGA GCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACCCTG AGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAGAAG GATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAAAGG GCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCCACA TGCAAGCCCTGCCACCTAGG Clone RY-26568 CAR LxH (SEQ ID NO: 368) MALPVTALLL PLALLLHAAR PDIQLTQSPS SVSASVGDRV TITCRASRGI SSWLAWYQQK PGKAPKLLIY GASSLQSGVP SRFSGSGSGT DFTLTISSLQ PEDFATYYCQ QIYTFPFTFG GGTKVEIKRG STSGSGKPGS GEGSTKGQVQ LVESGGGVVQ PGRSLRLSCA ASGFTFGSYG MHWVRQAPGK GLEWVAVIHY DGSVEYYADS VKGRFTISRD NSKDTLYLQM NSLRAEDTAV YYCARTDFWS GSPPSLDYWG QGTLVTVSSA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR Clone PP-26575 HC DNA (SEQ ID NO: 369) CAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGTCCTCGGTGAAGGTCTC CTGCAAGGCTTCTGGAGGCACCCTCAGCAGCCTGGCTATCAGCTGGGTGCGACAGGCCCCTG GACAAGGGCTTGAGTGGATGGGAGGGGTCATCCCTATCTTGGGTCGGGCAAACTACGCACAG AAGTTCCAGGGCAGAGTCACGATTACCGCGGACGAGTCCACGAGCACAGCCTACATGGAGCT GAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAACTCCTGAATACTCCT CCAGCATATGGCACTATTACTACGGCATGGACGTATGGGGCCAGGGAACAACTGTCACCGTC TCCTCA Clone PP-26575 HC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 370) QVQLVQSGAEVKKPGSSVKVSCKASGGTLSSLAISWVRQAPGQGLEWMGGVIPILGRANYAQ KFQGRVTITADESTSTAYMELSSLRSEDTAVYYCARTPEYSSSIWHYYYGMDVWGQGTTVTV SS (SEQ ID NO: 371) GTLSSLAIS (HC CDR1) (SEQ ID NO: 372) GVIPILGRANYAQKFQG (HC CDR2) (SEQ ID NO: 373) ARTPEYSSSIWHYYYGMDV (HC CDR3) Clone PP-26575 LC DNA (SEQ ID NO: 374) GACATCGTGATGACCCAGTCTCCAGACTCCCTGGCTGTGTCTCTGGGCGAGAGGGCCACCAT CAACTGCAAGTCCAGCCAGAGTGTTTTATACAGCTCCAACAATAAGAACTACTTAGCTTGGT ACCAGCAGAAACCAGGACAGCCTCCTAAGCTGCTCATTTACTGGGCATCTACCCGGGAATCC GGGGTCCCTGACCGATTCAGTGGCAGCGGGTCTGGGACAGATTTCACTCTCACCATCAGCAG CCTGCAGGCTGAAGATGTGGCAGTTTATTACTGTCAGCAGTTCGCCCACACTCCTTTCACTT TTGGCGGAGGGACCAAGGTTGAGATCAAACGG Clone PP-26575 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 375) DIVMTQSPDSLAVSLGERATINCKSSQSVLYSSNNKNYLAWYQQKPGQPPKLLIYWASTR ESGVPDRFSGSGSGTDFTLTISSLQAEDVAVYYCQQFAHTPFTFGGGTKVEIKR (SEQ ID NO: 376) KSSQSVLYSSNNKNYLA (LC CDR1) (SEQ ID NO: 377) WASTRES (LC CDR2) (SEQ ID NO: 378) QQFAHTPFT (LC CDR3) Clone PP-26575 CAR DNA HxL (SEQ ID NO: 379) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAGCCTGGGTCCTCGGTGAAGGTCT CCTGCAAGGCTTCTGGAGGCACCCTCAGCAGCCTGGCTATCAGCTGGGTGCGACAGGCCCCT GGACAAGGGCTTGAGTGGATGGGAGGGGTCATCCCTATCTTGGGTCGGGCAAACTACGCACA GAAGTTCCAGGGCAGAGTCACGATTACCGCGGACGAGTCCACGAGCACAGCCTACATGGAGC TGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTACTGCGCCAGAACTCCTGAATACTCC TCCAGCATATGGCACTATTACTACGGCATGGACGTATGGGGCCAGGGAACAACTGTCACCGT CTCCTCAGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGG ACATCGTGATGACCCAGTCTCCAGACTCCCTGGCTGTGTCTCTGGGCGAGAGGGCCACCATC AACTGCAAGTCCAGCCAGAGTGTTTTATACAGCTCCAACAATAAGAACTACTTAGCTTGGTA CCAGCAGAAACCAGGACAGCCTCCTAAGCTGCTCATTTACTGGGCATCTACCCGGGAATCCG GGGTCCCTGACCGATTCAGTGGCAGCGGGTCTGGGACAGATTTCACTCTCACCATCAGCAGC CTGCAGGCTGAAGATGTGGCAGTTTATTACTGTCAGCAGTTCGCCCACACTCCTTTCACTTT TGGCGGAGGGACCAAGGTTGAGATCAAACGGGCCGCTGCCCTTGATAATGAAAAGTCAAACG GAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCC AAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCAC CGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACA TGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCT AGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGAAGAGTATGACG TTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACCCC CAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGG CATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTG CTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG Clone PP-26575 CAR HxL (SEQ ID NO: 380) MALPVTALLL PLALLLHAAR PQVQLVQSGA EVKKPGSSVK VSCKASGGTL SSLAISWVRQ APGQGLEWMG GVIPILGRAN YAQKFQGRVT ITADESTSTA YMELSSLRSE DTAVYYCART PEYSSSIWHY YYGMDVWGQG TTVTVSSGST SGSGKPGSGE GSTKGDIVMT QSPDSLAVSL GERATINCKS SQSVLYSSNN KNYLAWYQQK PGQPPKLLIY WASTRESGVP DRFSGSGSGT DFTLTISSLQ AEDVAVYYCQ QFAHTPFTFG GGTKVEIKRA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR Clone PP-26575 CAR DNA LxH (SEQ ID NO: 381) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGACATCGTGATGACCCAGTCTCCAGACTCCCTGGCTGTGTCTCTGGGCGAGAGGGCCACCA TCAACTGCAAGTCCAGCCAGAGTGTTTTATACAGCTCCAACAATAAGAACTACTTAGCTTGG TACCAGCAGAAACCAGGACAGCCTCCTAAGCTGCTCATTTACTGGGCATCTACCCGGGAATC CGGGGTCCCTGACCGATTCAGTGGCAGCGGGTCTGGGACAGATTTCACTCTCACCATCAGCA GCCTGCAGGCTGAAGATGTGGCAGTTTATTACTGTCAGCAGTTCGCCCACACTCCTTTCACT TTTGGCGGAGGGACCAAGGTTGAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGG AAGTGGCGAAGGTAGTACAAAGGGGCAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGA AGCCTGGGTCCTCGGTGAAGGTCTCCTGCAAGGCTTCTGGAGGCACCCTCAGCAGCCTGGCT ATCAGCTGGGTGCGACAGGCCCCTGGACAAGGGCTTGAGTGGATGGGAGGGGTCATCCCTAT CTTGGGTCGGGCAAACTACGCACAGAAGTTCCAGGGCAGAGTCACGATTACCGCGGACGAGT CCACGAGCACAGCCTACATGGAGCTGAGCAGCCTGAGATCTGAGGACACGGCGGTGTACTAC TGCGCCAGAACTCCTGAATACTCCTCCAGCATATGGCACTATTACTACGGCATGGACGTATG GGGCCAGGGAACAACTGTCACCGTCTCCTCAGCCGCTGCCCTTGATAATGAAAAGTCAAACG GAACAATCATTCACGTGAAGGGCAAGCACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCC AAGCCATTCTGGGTGTTGGTCGTAGTGGGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCAC CGTGGCTTTTATAATCTTCTGGGTTAGATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACA TGAATATGACTCCACGCCGCCCTGGCCCCACAAGGAAACACTACCAGCCTTACGCACCACCT AGAGATTTCGCTGCCTATCGGAGCAGGGTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTA TCAGCAGGGCCAGAACCAACTGTATAACGAGCTCAACCTGGGACGCAGGGAAGAGTATGACG TTTTGGACAAGCGCAGAGGACGGGACCCTGAGATGGGTGGCAAACCAAGACGAAAAAACCCC CAGGAGGGTCTCTATAATGAGCTGCAGAAGGATAAGATGGCTGAAGCCTATTCTGAAATAGG CATGAAAGGAGAGCGGAGAAGGGGAAAAGGGCACGACGGTTTGTACCAGGGACTCAGCACTG CTACGAAGGATACTTATGACGCTCTCCACATGCAAGCCCTGCCACCTAGG Clone PP-26575 CAR LxH (SEQ ID NO: 382) MALPVTALLL PLALLLHAAR PDIVMTQSPD SLAVSLGERA TINCKSSQSV LYSSNNKNYL AWYQQKPGQP PKLLIYWAST RESGVPDRFS GSGSGTDFTL TISSLQAEDV AVYYCQQFAH TPFTFGGGTK VEIKRGSTSG SGKPGSGEGS TKGQVQLVQS GAEVKKPGSS VKVSCKASGG TLSSLAISWV RQAPGQGLEW MGGVIPILGR ANYAQKFQGR VTITADESTS TAYMELSSLR SEDTAVYYCA RTPEYSSSIW HYYYGMDVWG QGTTVTVSSA AALDNEKSNG TIIHVKGKHL CPSPLFPGPS KPFWVLVVVG GVLACYSLLV TVAFIIFWVR SKRSRLLHSD YMNMTPRRPG PTRKHYQPYA PPRDFAAYRS RVKFSRSADA PAYQQGQNQL YNELNLGRRE EYDVLDKRRG RDPEMGGKPR RKNPQEGLYN ELQKDKMAEA YSEIGMKGER RRGKGHDGLY QGLSTATKDT YDALHMQALP PR Clone RD-26576 HC DNA (SEQ ID NO: 383) CAGGTGCGGCTGGTGGAGTCTGGGGGGGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACTCTC CTGTGCAGCGTCTGGATTCACCTTCAGTAGCTATGGCATACACTGGGTCCGCCAGGCTCCAG GCAAGGGGCTGGAGTGGGTGGCAGTTATAGGGTATGATGGACAGGAGAAATACTATGCAGAC TCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAAT GAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCGTTGCAGGAGC CGCCATACGCTTTTGGGATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCA Clone RD-26576 HC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 384) QVRLVESGGGVVQPGRSLRLSCAASGFTFSSYGIHWVRQAPGKGLEWVAVIGYDGQEKYYAD SVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCVKGPLQEPPYAFGMDVWGQGTTVTVSS (SEQ ID NO: 385) FTFSSYGIH (HC CDR1) (SEQ ID NO: 386) VIGYDGQEKYYADSVKG (HC CDR2) (SEQ ID NO: 387) VKGPLQEPPYAFGMDV (HC CDR3) Clone RD-26576 LC DNA (SEQ ID NO: 388) GAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCT CTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCC AGGCTCCCAGGCTCCTCATCTATAGCGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTC AGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATTT TGCAGTTTATTACTGTCAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGAGGGACCAAGG TTGAGATCAAACGG Clone RD-26576 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 389) EIVMTQSPATLSVSPGERATLSCRASQSVSSNLAWYQQKPGQAPRLLIYSASTRATGIPA RFSGSGSGTEFTLTISSLQSEDFAVYYCQQHHVWPLTFGGGTKVEIKR (SEQ ID NO: 390) RASQSVSSNLA (LC CDR1) (SEQ ID NO: 391) SASTRAT (LC CDR2) (SEQ ID NO: 392) QQHHVWPLT (LC CDR3) Clone RD-26576 CAR DNA HxL (SEQ ID NO: 393) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GCAGGTGCGGCTGGTGGAGTCTGGGGGGGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACTCT CCTGTGCAGCGTCTGGATTCACCTTCAGTAGCTATGGCATACACTGGGTCCGCCAGGCTCCA GGCAAGGGGCTGGAGTGGGTGGCAGTTATAGGGTATGATGGACAGGAGAAATACTATGCAGA CTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAA TGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCGTTGCAGGAG CCGCCATACGCTTTTGGGATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCAGG GTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATAGTGA TGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGG GCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAG GCTCCTCATCTATAGCGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTCAGTGGCAGTG GGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATTTTGCAGTTTAT TACTGTCAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGAGGGACCAAGGTTGAGATCAA ACGGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGC ACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTG GGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAG ATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCC CCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGG GTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAA CGAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACC CTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAG AAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAA AGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCC ACATGCAAGCCCTGCCACCTAGG Clone RD-26576 CAR HxL (SEQ ID NO: 394) MALPVTALLL PLALLLHAAR PQVRLVESGG GVVQPGRSLR LSCAASGFTF SSYGIHWVRQ APGKGLEWVA VIGYDGQEKY YADSVKGRET ISRDNSKNTL YLQMNSLRAE DTAVYYCVKG PLQEPPYAFG MDVWGQGTTV TVSSGSTSGS GKPGSGEGST KGEIVMTQSP ATLSVSPGER ATLSCRASQS VSSNLAWYQQ KPGQAPRLLI YSASTRATGI PARFSGSGSG TEFTLTISSL QSEDFAVYYC QQHHVWPLTF GGGTKVEIKR AAALDNEKSN GTIIHVKGKH LCPSPLFPGP SKPFWVLVVV GGVLACYSLL VTVAFIIFWV RSKRSRLLHS DYMNMTPRRP GPTRKHYQPY APPRDFAAYR SRVKFSRSAD APAYQQGQNQ LYNELNLGRR EEYDVLDKRR GRDPEMGGKP RRKNPQEGLY NELQKDKMAE AYSEIGMKGE RRRGKGHDGL YQGLSTATKD TYDALHMQAL PPR Clone RD-26576 CAR DNA LxH (SEQ ID NO: 395) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCC TCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGC CAGGCTCCCAGGCTCCTCATCTATAGCGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTT CAGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATT TTGCAGTTTATTACTGTCAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGAGGGACCAAG GTTGAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTAC AAAGGGGCAGGTGCGGCTGGTGGAGTCTGGGGGGGGCGTGGTCCAGCCTGGGAGGTCCCTGA GACTCTCCTGTGCAGCGTCTGGATTCACCTTCAGTAGCTATGGCATACACTGGGTCCGCCAG GCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTTATAGGGTATGATGGACAGGAGAAATACTA TGCAGACTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATC TGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCGTTG CAGGAGCCGCCATACGCTTTTGGGATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTC CTCAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGC ACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTG GGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAG ATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCC CCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGG GTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAA CGAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACC CTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAG AAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAA AGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCC ACATGCAAGCCCTGCCACCTAGG Clone RD-26576 CAR LxH (SEQ ID NO: 396) MALPVTALLL PLALLLHAAR PEIVMTQSPA TLSVSPGERA TLSCRASQSV SSNLAWYQQK PGQAPRLLIY SASTRATGIP ARFSGSGSGT EFTLTISSLQ SEDFAVYYCQ QHHVWPLTFG GGTKVEIKRG STSGSGKPGS GEGSTKGQVR LVESGGGVVQ PGRSLRLSCA ASGFTFSSYG IHWVRQAPGK GLEWVAVIGY DGQEKYYADS VKGRFTISRD NSKNTLYLQM NSLRAEDTAV YYCVKGPLQE PPYAFGMDVW GQGTTVTVSS AAALDNEKSN GTIIHVKGKH LCPSPLFPGP SKPFWVLVVV GGVLACYSLL VTVAFIIFWV RSKRSRLLHS DYMNMTPRRP GPTRKHYQPY APPRDFAAYR SRVKFSRSAD APAYQQGQNQ LYNELNLGRR EEYDVLDKRR GRDPEMGGKP RRKNPQEGLY NELQKDKMAE AYSEIGMKGE RRRGKGHDGL YQGLSTATKD TYDALHMQAL PPR Clone RD-26578 HC DNA (SEQ ID NO: 397) CAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACTCTC CTGTGCAGCGTCTGGATTCACCTTCAGTAGCCGTGGCATGCACTGGGTCCGCCAGGCTCCAG GCAAGGGGCTGGAGTGGGTGGCAGTTATAGGGTATGATGGACAGGAGAAATACTATGCAGAC TCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAAT GAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCGTTGCAGGAGC CGCCATACGATTATGGAATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCA Clone RD-26578 HC CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 398) QVQLVESGGGVVQPGRSLRLSCAASGFTFSSRGMHWVRQAPGKGLEWVAVIGYDGQEKYYAD SVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCVKGPLQEPPYDYGMDVWGQGTTVTVSS (SEQ ID NO: 399)  FTFSSRGMH (HC CDR1) (SEQ ID NO: 400) VIGYDGQEKYYADSVKG (HC CDR2) (SEQ ID NO: 401) VKGPLQEPPYDYGMDV (HC CDR3) Clone RD-26578 LC DNA (SEQ ID NO: 402) GAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCT CTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCC AGGCTCCCAGGCTCCTCATCTATAGCGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTC AGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATTT TGCAGTTTATTACTGTCAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGAGGGACCAAGG TTGAGATCAAACGG Clone RD-26578 LC. CDRs 1, 2, and 3 are underlined. (SEQ ID NO: 403) EIVMTQSPATLSVSPGERATLSCRASQSVSSNLAWYQQKPGQAPRLLIYS ASTRATGIPARFSGSGSGTEFTLTISSLQSEDFAVYYCQQHHVWPLTFGGGTKVEIKR (SEQ ID NO: 404) RASQSVSSNLA (LC CDR1) (SEQ ID NO: 405) SASTRAT (LC CDR2) (SEQ ID NO: 406) QQHHVWPLT (LC CDR3) Clone RD-26578 CAR DNA HxL (SEQ ID NO: 407) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGAGACTCT CCTGTGCAGCGTCTGGATTCACCTTCAGTAGCCGTGGCATGCACTGGGTCCGCCAGGCTCCA GGCAAGGGGCTGGAGTGGGTGGCAGTTATAGGGTATGATGGACAGGAGAAATACTATGCAGA CTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAA TGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCGTTGCAGGAG CCGCCATACGATTATGGAATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTCCTCAGG GTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTACAAAGGGGGAAATAGTGA TGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCAGG GCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAG GCTCCTCATCTATAGCGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTTCAGTGGCAGTG GGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATTTTGCAGTTTAT TACTGTCAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGAGGGACCAAGGTTGAGATCAA ACGGGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGC ACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTG GGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAG ATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCC CCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGG GTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAA CGAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACC CTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAG AAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAA AGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCC ACATGCAAGCCCTGCCACCTAGG Clone RD-26578 CAR HxL (SEQ ID NO: 408) MALPVTALLL PLALLLHAAR PQVQLVESGG GVVQPGRSLR LSCAASGFTF SSRGMHWVRQ APGKGLEWVA VIGYDGQEKY YADSVKGRFT ISRDNSKNTL YLQMNSLRAE DTAVYYCVKG PLQEPPYDYG MDVWGQGTTV TVSSGSTSGS GKPGSGEGST KGEIVMTQSP ATLSVSPGER ATLSCRASQS VSSNLAWYQQ KPGQAPRLLI YSASTRATGI PARFSGSGSG TEFTLTISSL QSEDFAVYYC QQHHVWPLTF GGGTKVEIKR AAALDNEKSN GTIIHVKGKH LCPSPLFPGP SKPFWVLVVV GGVLACYSLL VTVAFIIFWV RSKRSRLLHS DYMNMTPRRP GPTRKHYQPY APPRDFAAYR SRVKFSRSAD APAYQQGQNQ LYNELNLGRR EEYDVLDKRR GRDPEMGGKP RRKNPQEGLY NELQKDKMAE AYSEIGMKGE RRRGKGHDGL YQGLSTATKD TYDALHMQAL PPR Clone RD-26578 CAR DNA LxH (SEQ ID NO: 409) ATGGCACTCCCCGTAACTGCTCTGCTGCTGCCGTTGGCATTGCTCCTGCACGCCGCACGCCC GGAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCC TCTCCTGCAGGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGC CAGGCTCCCAGGCTCCTCATCTATAGCGCATCCACCAGGGCCACTGGTATCCCAGCCAGGTT CAGTGGCAGTGGGTCTGGGACAGAGTTCACTCTCACCATCAGCAGCCTGCAGTCTGAAGATT TTGCAGTTTATTACTGTCAGCAGCACCACGTCTGGCCTCTCACTTTTGGCGGAGGGACCAAG GTTGAGATCAAACGGGGGTCTACATCCGGCTCCGGGAAGCCCGGAAGTGGCGAAGGTAGTAC AAAGGGGCAGGTGCAGCTGGTGGAGTCTGGGGGAGGCGTGGTCCAGCCTGGGAGGTCCCTGA GACTCTCCTGTGCAGCGTCTGGATTCACCTTCAGTAGCCGTGGCATGCACTGGGTCCGCCAG GCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTTATAGGGTATGATGGACAGGAGAAATACTA TGCAGACTCCGTGAAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATC TGCAAATGAACAGCCTGAGAGCCGAGGACACGGCGGTGTACTACTGCGTCAAGGGGCCGTTG CAGGAGCCGCCATACGATTATGGAATGGACGTATGGGGCCAGGGAACAACTGTCACCGTCTC CTCAGCCGCTGCCCTTGATAATGAAAAGTCAAACGGAACAATCATTCACGTGAAGGGCAAGC ACCTCTGTCCGTCACCCTTGTTCCCTGGTCCATCCAAGCCATTCTGGGTGTTGGTCGTAGTG GGTGGAGTCCTCGCTTGTTACTCTCTGCTCGTCACCGTGGCTTTTATAATCTTCTGGGTTAG ATCCAAAAGAAGCCGCCTGCTCCATAGCGATTACATGAATATGACTCCACGCCGCCCTGGCC CCACAAGGAAACACTACCAGCCTTACGCACCACCTAGAGATTTCGCTGCCTATCGGAGCAGG GTGAAGTTTTCCAGATCTGCAGATGCACCAGCGTATCAGCAGGGCCAGAACCAACTGTATAA CGAGCTCAACCTGGGACGCAGGGAAGAGTATGACGTTTTGGACAAGCGCAGAGGACGGGACC CTGAGATGGGTGGCAAACCAAGACGAAAAAACCCCCAGGAGGGTCTCTATAATGAGCTGCAG AAGGATAAGATGGCTGAAGCCTATTCTGAAATAGGCATGAAAGGAGAGCGGAGAAGGGGAAA AGGGCACGACGGTTTGTACCAGGGACTCAGCACTGCTACGAAGGATACTTATGACGCTCTCC ACATGCAAGCCCTGCCACCTAGG Clone RD-26578 CAR LxH (SEQ ID NO: 410) MALPVTALLL PLALLLHAAR PEIVMTQSPA TLSVSPGERA TLSCRASQSV SSNLAWYQQK PGQAPRLLIY SASTRATGIP ARFSGSGSGT EFTLTISSLQ SEDFAVYYCQ QHHVWPLTFG GGTKVEIKRG STSGSGKPGS GEGSTKGQVQ LVESGGGVVQ PGRSLRLSCA ASGFTFSSRG MHWVRQAPGK GLEWVAVIGY DGQEKYYADS VKGRFTISRD NSKNTLYLQM NSLRAEDTAV YYCVKGPLQE PPYDYGMDVW GQGTTVTVSS AAALDNEKSN GTIIHVKGKH LCPSPLFPGP SKPFWVLVVV GGVLACYSLL VTVAFIIFWV RSKRSRLLHS DYMNMTPRRP GPTRKHYQPY APPRDFAAYR SRVKFSRSAD APAYQQGQNQ LYNELNLGRR EEYDVLDKRR GRDPEMGGKP RRKNPQEGLY NELQKDKMAE AYSEIGMKGE RRRGKGHDGL YQGLSTATKD TYDALHMQAL PPR 

What is claimed is:
 1. A polypeptide comprising an antigen binding molecule that specifically binds to B-cell maturation antigen (BCMA), wherein the antigen binding molecule comprises a VH CDR1 region comprising the amino acid sequence of SEQ ID NO: 399; a VH CDR2 region comprising the amino acid sequence of SEQ ID NO: 400; a VH CDR3 region comprising the amino acid sequence of SEQ ID NO: 401; a VL CDR1 region comprising the amino acid sequence of SEQ ID NO: 404; a VL CDR2 region comprising the amino acid sequence of SEQ ID NO: 405; and a VL CDR3 region comprising the amino acid sequence of SEQ ID NO:
 406. 2. The polypeptide of claim 1, wherein the antigen binding molecule comprises a VH comprising the amino acid sequence of SEQ ID NO: 398; and a VL comprising the amino acid sequence of SEQ ID NO:
 403. 3. The polypeptide of claim 1, wherein the antigen binding molecule is selected from the group consisting of scFv, Fab, Fab′, Fv, F(ab′)2, and any combination thereof.
 4. The polypeptide of claim 3, wherein the antigen binding molecule comprises an scFv and the VH and the VL are connected by a linker.
 5. The polypeptide of claim 4, wherein the linker comprises an amino acid sequence at least 85% identical to the amino acid sequence of SEQ ID NO:
 174. 6. The polypeptide of claim 1, wherein the polypeptide is a chimeric antigen receptor (CAR) or a T cell receptor (TCR).
 7. The polypeptide of claim 6, wherein the CAR or TCR further comprises a transmembrane domain.
 8. The polypeptide of claim 7, wherein the transmembrane domain is a transmembrane domain of CD28, 4-1BB, CD8 alpha, CD4, CD19, CD3 epsilon, CD45, CD5, CD9, CD16, CD22, CD33, CD37, CD64, CD80, CD86, CD134, CD137, CD154, an alpha chain of a T cell receptor, a beta chain of a T cell receptor, a zeta chain of a T cell receptor, or any combination thereof.
 9. The polypeptide of claim 7, wherein the CAR further comprises a hinge region between the transmembrane domain and the antigen binding molecule, wherein the hinge region is of IgG1, IgG2, IgG3, IgG4, IgA, IgD, IgE, IgM, CD28, or CD8 alpha.
 10. The polypeptide of claim 6, wherein the CAR or TCR further comprises a costimulatory region, wherein the costimulatory region is a signaling region of CD28, OX-40, 4-1BB, CD2, CD7, CD27, CD30, CD40, PD-1, ICOS, LFA-1, CD11α, CD3 gamma, CD3 delta, CD3 epsilon, CD247, CD276, LIGHT, NKG2C, Ig alpha, DAP-10, Fc gamma receptor, MHC class I molecule, TNF receptor proteins, Immunoglobulin-like proteins, cytokine receptors, integrins, signaling lymphocytic activation molecules, activating NK cell receptors, BTLA, a Toll ligand receptor, B7-H3, CDS, GITR, BAFFR, HVEM, KIRDS2, SLAMF7, NKp80, NKp44, NKp30, NKp46, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, ITGAE, ITGAL, ITGAM, ITGAX, ITGB1, CD29, ITGB2, CD18, ITGB7, NKG2D, TNFR2, TRANCE, DNAM1, SLAMF4, CD84, CD96, CEACAM1, CRTAM, Ly9, CD160, PSGL1, CD100, CD69, SLAMF6, SLAM, BLAME, SELPLG, LTBR, LAT, GADS, SLP-76, PAG, CD19a, a ligand that specifically binds with CD83, or any combination thereof.
 11. The polypeptide of claim 6, wherein the CAR or TCR further comprises an activation domain.
 12. The polypeptide of claim 11, wherein the activation domain is a CD3 zeta domain.
 13. One or more polynucleotide(s) encoding the polypeptide of claim
 1. 14. A cell comprising the polypeptide(s) of claim
 13. 15. The cell of claim 14, which is a tumor-infiltrating lymphocyte (TIL), autologous T cell, engineered autologous T cell (eACT), or an allogeneic T cell.
 16. A composition comprising the cell of claim 14 and a carrier.
 17. A method of preparing a transduced cell, comprising introducing the one or more polynucleotide(s) of claim 13 into a cell.
 18. A method for inducing immunity against a tumor in a subject in need thereof, comprising administering to the subject the polypeptide of claim 1 or a cell expressing the polypeptide.
 19. A method for treating a cancer in a subject in need thereof, comprising administering to the subject the polypeptide of claim 1 or a cell expressing the polypeptide.
 20. The method of claim 19, wherein the cancer is multiple myeloma, Hodgkin's Disease, non-Hodgkin's lymphoma (NHL), primary mediastinal large B cell lymphoma (PMBC), diffuse large B cell lymphoma (DLBCL), follicular lymphoma (FL), transformed follicular lymphoma, splenic marginal zone lymphoma (SMZL), chronic or acute leukemia, acute myeloid leukemia, chronic myeloid leukemia, acute lymphoblastic leukemia (ALL), chronic lymphocytic leukemia (CLL), T-cell lymphoma, one or more of B-cell acute lymphoid leukemia (BALL), T-cell acute lymphoid leukemia (TALL), acute lymphoid leukemia (ALL), chronic myelogenous leukemia (CIVIL), B cell prolymphocytic leukemia, blastic plasmacytoid dendritic cell neoplasm, Burkitt's lymphoma, diffuse large B cell lymphoma, follicular lymphoma, hairy cell leukemia, small cell- or a large cell-follicular lymphoma, malignant lymphoproliferative conditions, MALT lymphoma, mantle cell lymphoma, Marginal zone lymphoma, myelodysplasia and myelodysplastic syndrome, plasmablastic lymphoma, plasmacytoid dendritic cell neoplasm, Waldenstrom macroglobulinemia, a plasma cell proliferative disorder, asymptomatic myeloma, smoldering multiple myeloma, indolent myeloma, monoclonal gammapathy of undetermined significance (MGUS), plasmacytomas, plasma cell dyscrasia, solitary myeloma, solitary plasmacytoma, extramedullary plasmacytoma, multiple plasmacytoma, systemic amyloid light chain amyloidosis, POEMS syndrome, or a combination thereof. 